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291.
公开(公告)号:WO2013150840A1
公开(公告)日:2013-10-10
申请号:PCT/JP2013/055148
申请日:2013-02-27
Applicant: 宇部興産株式会社
IPC: C07C201/04 , C07C203/00 , C07B61/00 , C07C67/18 , C07C67/36 , C07C69/36 , C07C69/96
CPC classification number: C07C201/04 , C07C67/36 , C07C68/00 , C07C69/96 , C07C69/36 , C07C203/00
Abstract: 一酸化窒素と酸素とアルコールとを反応させて亜硝酸エステルを生成させる亜硝酸エステルの製造方法であって、上記反応塔の底部からの塔底液と、一酸化窒素及び/又は一酸化炭素とを反応器に供給して亜硝酸エステルを生成させる工程と、亜硝酸エステルを反応塔に供給する工程と、反応器から水と硝酸とアルコールとを含有する反応液を硝酸濃縮塔に供給する工程と、硝酸濃縮塔において、硝酸濃縮塔の底部に生じる濃縮液中のアルコール濃度を4.0重量%未満に制御しながら、反応液から低沸点分を蒸留分離して、硝酸濃縮塔の下部から、濃縮液を反応器に導入する工程と、を有する亜硝酸エステルの製造方法である。
Abstract translation: 一种用于生产亚硝酸酯的方法,其中使一氧化氮,氧和醇反应以产生亚硝酸酯,所述产生亚硝酸酯的方法包括:从反应塔底部供应底部液体的步骤 ,和一氧化氮和/或一氧化碳转化成反应器以产生亚硝酸酯; 将亚硝酸酯供应到反应塔的步骤; 从反应器将含有水,硝酸和醇的反应液供给到硝酸浓缩塔的步骤; 以及通过蒸馏将低沸点馏分与反应液分离的步骤,同时控制硝酸浓缩塔底部产生的浓缩液中的醇浓度小于4.0重量%,将浓缩液引入反应器 。
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292.
公开(公告)号:JP6070695B2
公开(公告)日:2017-02-01
申请号:JP2014509081
申请日:2013-02-27
Applicant: 宇部興産株式会社
IPC: C07C203/00 , C07C69/36 , C07C69/96 , C07C68/00 , C07C201/04
CPC classification number: C07C201/04 , C07C67/36 , C07C68/00
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公开(公告)号:JP5191477B2
公开(公告)日:2013-05-08
申请号:JP2009500332
申请日:2007-03-14
Applicant: ラーシュ・エー・グスタフソンLars E. GUSTAFSSON , ダグ・リンナショーンDag LINNARSSON , クリストファー・ニルソンKristofer NILSSON
Inventor: ラーシュ・エー・グスタフソン , ダグ・リンナショーン , クリストファー・ニルソン
IPC: C07C201/04 , A61J1/00 , A61K31/21 , A61K47/10 , A61K47/26 , A61K47/34 , A61K47/36 , A61P1/04 , A61P3/12 , A61P9/00 , A61P9/04 , A61P9/06 , A61P9/10 , A61P9/12 , A61P11/00 , A61P11/06 , A61P13/02 , A61P13/10 , A61P17/00 , A61P17/02 , A61P17/06 , A61P21/00 , A61P25/00 , A61P29/00 , A61P35/00 , C07C203/00
CPC classification number: C07C201/04 , C07B43/02 , C07C203/00
Abstract: Organic nitrites can be produced from a compound which is a mono/polyhydric alcohol or an aldehyde- or ketone-derivate thereof after de-aeration of the same, using NO gas, and stored in an environment saturated with gaseous NO. Organic nitrites produced according to the invention exhibit less impurities and improved storage stability compared to conventionally produced nitrites. The organic nitrites of the invention can easily be formulated into pharmaceutical compositions and have utility for the treatment of various conditions.
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公开(公告)号:JP2011236209A
公开(公告)日:2011-11-24
申请号:JP2011090875
申请日:2011-04-15
Applicant: China Petroleum & Chemical Corp , Shanghai Research Inst Of Petrochemical Technology Sinopec , 中国石油化工股▲ふん▼有限公司 , 中國石油化工股▲フン▼有限公司上海石油化工研究院
Inventor: LIU JUNTAO , LI SIQIN , LI LEI , ZHANG LINNA
IPC: C07C201/04 , C07B61/00 , C07C203/04
CPC classification number: C07C201/04 , C07C203/00
Abstract: PROBLEM TO BE SOLVED: To provide a new method for producing C-Calkyl nitrite having advantage of high selectivity of C-Calkyl nitrite.SOLUTION: This method for producing C-Calkyl nitrite includes processes for: loading a resin catalyst layer and/or a porous filler layer into a reactor; passing nitrogen oxide, oxygen and C-Calcohol as raw materials through the resin catalyst layer and/or porous filler layer in a counter current, parallel current or cross current manner; and reacting under the reaction conditions including a reaction temperature of 0-150°C, a reaction pressure of -0.09 to 1.5 MPa, a molar ratio of C-Calkanol/nitrogen oxide of 1-100:1, a molar ratio of nitrogen oxide/oxygen of 4-50:1, to obtain waste liquid containing C-Calkyl nitrite; wherein the nitrogen oxide is NO, or a mixed gas containing NO and one or more selected from NOand NO.
Abstract translation: 要解决的问题:提供一种新方法,用于生产具有优势的C
1 SB> 选择性C 1 SB> -C 4 SB>亚硝酸烷基酯。 解决方案:用于生产C
1 SB> -C 4 SB>亚硝酸烷基酯的方法包括以下步骤:将树脂催化剂层和 /或多孔填料层进入反应器; 通过树脂催化剂层和/或多孔填料层作为原料通过氮氧化物,氧气和C 1 SB> -C 4 SB> 以逆流,并联电流或交叉电流方式; 在反应温度0〜150℃,反应压力-0.09〜1.5MPa,摩尔比C 1 SB> -C 4 SB>链烷醇/氮氧化物为1-100:1,氮氧化物/氧气的摩尔比为4-50:1,得到含有C 1 SB> -C 4 SB>亚硝酸烷基酯; 其中氮氧化物为NO,或含有NO的混合气体和选自N 3 SB>和NO < SB POS =“POST”> 2 SB>。 版权所有(C)2012,JPO&INPIT -
公开(公告)号:JP2005536558A
公开(公告)日:2005-12-02
申请号:JP2004532054
申请日:2003-08-06
Applicant: ニコックス エス エイ
Inventor: サンタス,ジャンカルロ , ソルダト,ピエロ デル , ベネディニ,フランセスカ
IPC: A61K31/618 , A61K31/216 , C07B61/00 , C07C67/10 , C07C69/734 , C07C201/02 , C07C201/04 , C07C201/08 , C07C203/00 , C07C203/04 , C07C269/06 , C07C271/28
CPC classification number: C07C269/06 , C07C67/10 , C07C69/734 , C07C201/02 , C07C203/04 , C07C271/28 , C07C303/28 , C07C309/73
Abstract: The present invention refers to a process for preparing a compound of general formula (A), as reported in the description, wherein R is a radical of a drug and R1-R12 are hydrogen or alkyl groups, m, n, o, q, r and s are each independently an integer from 0 to 6, and p is 0 or 1, and X is O, S, SO, SO2, NR13 or PR13 or an aryl, heteroaryl group, said process comprising reacting a compound of formula (B) R—COOZ (B) wherein R is as defined above and Z is hydrogen or a cation selected from: Li+, Na+, K+, Ca++, Mg++, tetralkylammonium, tetralkylphosphonium, with a compound of formula (C), as reported in the description, wherein R1-R12 and m, n, o, p, q, r, s are as defined above and Y is a suitable leaving group.
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公开(公告)号:JP2003261515A
公开(公告)日:2003-09-19
申请号:JP2002060376
申请日:2002-03-06
Applicant: UBE INDUSTRIES
Inventor: TANAKA HIDEJI , II HIROFUMI , MITSUI KAZUAKI
IPC: C07C201/04 , C07B61/00 , C07C203/00
Abstract: PROBLEM TO BE SOLVED: To provide a method for efficiently producing an alkyl nitrite in higher yield by reaction between nitrogen dioxide and an alkanol. SOLUTION: The method for producing the alkyl nitrite comprises feeding a reaction column with the alkanol and water to allow them to flow down and countercurrently contacting them with the nitrogen oxide while feeding it into the reaction column. More specifically, this method comprises the step (1) of introducing bottoms extracted from the bottom of the reaction column into a reactor, into which carbon monoxide or hydrogen is fed in the presence of a platinum metal catalyst and both the alkanol and nitric acid in the bottoms are reacted with the carbon monoxide or hydrogen to form the alkyl nitrite and the step (2) of feeding the alkyl nitrite into the zone where the alkanol in the reaction column is flowing down. COPYRIGHT: (C)2003,JPO
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公开(公告)号:JP2003128634A
公开(公告)日:2003-05-08
申请号:JP2001323123
申请日:2001-10-22
Applicant: UBE INDUSTRIES
Inventor: TANAKA HIDEJI , II HIROFUMI , MITSUI KAZUAKI
IPC: C07C201/04 , C07B61/00 , C07C203/04
Abstract: PROBLEM TO BE SOLVED: To provide an industrially preferable method for preparing an alkyl nitrite which is capable of preparing the alkyl nitrite easily and at a low cosy with a high efficiency. SOLUTION: The method for preparing the alkyl nitrite is characterized by reacting nitric acid and an alkanol, in the presence of a platinum group metal catalyst, with carbon monoxide or hydrogen. Further, a method for preparing the alkyl nitrite is characterized by using an aqueous solution containing nitric acid wherein the concentration of nitric acid is not higher than 60% by weight and contains 5 to 70% by weight of an alkanol, in the presence of the solid catalyst in which the platinum group metal or its compound is supported on the carrier, and the reaction is conducted until the concentration of nitric acid reaches not higher than 1% by weight.
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公开(公告)号:JPH08504191A
公开(公告)日:1996-05-07
申请号:JP51270194
申请日:1993-11-15
IPC: A61K31/21 , A61K31/215 , A61K31/38 , A61K31/381 , A61K31/40 , A61K31/403 , A61K31/4035 , A61K31/407 , A61P7/02 , A61P25/04 , A61P29/00 , A61P37/00 , C07C201/04 , C07C203/04 , C07C233/21 , C07C233/69 , C07C235/34 , C07C235/78 , C07C235/80 , C07D207/337 , C07D209/46 , C07D209/88 , C07D333/22 , C07D491/04 , C07D491/052
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公开(公告)号:JPH0723344B2
公开(公告)日:1995-03-15
申请号:JP24586588
申请日:1988-09-29
IPC: C07C201/16 , C07C67/00 , C07C201/00 , C07C201/04 , C07C203/00 , C07C203/02 , C07C203/04
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公开(公告)号:JPH0545576B2
公开(公告)日:1993-07-09
申请号:JP17946683
申请日:1983-09-29
Applicant: UNION CARBIDE CHEM PLASTIC
IPC: B01J23/00 , B01J23/44 , C07B61/00 , C07C67/00 , C07C67/36 , C07C69/36 , C07C201/00 , C07C201/04
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