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公开(公告)号:JPH06336464A
公开(公告)日:1994-12-06
申请号:JP11308994
申请日:1994-05-26
Applicant: RHONE POULENC CHIMIE
Inventor: PASUKARU METEIBIE , ROORAN BERUNAARU
IPC: C07C201/06 , C07C201/10 , C07C205/22 , C07C207/04
Abstract: The subject of the present invention is a process for the preparation of nitrophenols. More particularly, the invention relates to the preparation of p-nitrophenol. The process of preparation of the invention, which consists in preparing p-nitrophenol by nitrosation of phenol in the presence of sulphuric acid and then oxidation of p-nitrosophenol with nitric acid, is characterised in that, in the first nitrosation stage, the concentration of sulphuric acid is at least equal to 60% and, in the second stage, at the end of the oxidation reaction, the concentration of sulphuric acid is at most equal to 80%, which makes it possible to precipitate p-nitrophenol which is then separated.
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公开(公告)号:JPH03223235A
公开(公告)日:1991-10-02
申请号:JP23004090
申请日:1990-08-30
Applicant: TAOKA CHEMICAL CO LTD
Inventor: KIMURA OSAMU , HORIKAWA YASUHIKO , YAMASHITA MASAYA , MORINO KAZUKI , KOYAMA SHINICHI
IPC: B01J27/08 , B01J27/125 , B01J27/128 , C07B61/00 , C07C201/10 , C07C205/26 , C07C303/08 , C07C309/02 , C07C309/42
Abstract: PURPOSE:To obtain the title high purity compound industrially and advantageously by sulfonating 4-chloro-3-ethylphenol with chlorosulfonic acid in an organic solvent, chlorinating the reaction product and further nitrating the chlorinated substance with nitric acid. CONSTITUTION:4-Chloro-3-ethylphenol which is not required to separate isomers is sulfonated with chlorosulfonic acid in an organic solvent such as a halogenated hydrocarbon to industrially and advantageously give 5-chloro-4- ethyl-2-hydroxybenzenesulfonic acid. Then this compound is chlorinated in a solvent of acetic acid in the presence of sulfur chloride to industrially and advantageously give 3,5-dichloro-4-ethyl-2-hydroxybenzenesulfonic acid. Further, this compound is nitrated with nitric acid to industrially and advantageously give high-purity 2,4-dichloro-3-ethyl-6-nitrophenol useful as an intermediate for cyano coupler for color photography.
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公开(公告)号:JPH0354930B2
公开(公告)日:1991-08-21
申请号:JP17903284
申请日:1984-08-28
IPC: C07C205/26 , C07C67/00 , C07C201/00 , C07C201/10 , C07C213/00
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公开(公告)号:JPS6250459B2
公开(公告)日:1987-10-24
申请号:JP7373980
申请日:1980-06-03
Applicant: MITSUI TOATSU CHEMICALS
Inventor: TAKAGI USAJI , KASUGA TAKAHARU , TSUMURA RYUICHIRO
IPC: B01J31/00 , B01J31/02 , C07C67/00 , C07C201/00 , C07C201/10 , C07C205/02
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公开(公告)号:JPS60123450A
公开(公告)日:1985-07-02
申请号:JP22917683
申请日:1983-12-06
Applicant: UBE INDUSTRIES
Inventor: ITAYA HIROSHI , KASHIMA MIKITO , TAZAKI YASUTAKA
IPC: C07B43/02 , C07B31/00 , C07C67/00 , C07C201/00 , C07C201/10 , C07C205/06 , C07C205/37
Abstract: PURPOSE:To obtain the titled compound economically and advantageously in high selectivity, by reacting an aromatic iodine compound with nitrogen dioxide under mild conditions. CONSTITUTION:An aromatic iodine compound, e.g. mono- and diiodinated compound of an alkylbenzene, is reacted with nitrogen dioxide in a solvent, e.g. acetic acid or dichloromethane, at -10-+100 deg.C, preferably 0-60 deg.C to substitute the iodine ions with the nitrogen dioxide ions and give the aimed substance in the manner of position selectivity. The nitrogen dioxide to be used as an oxidizing agent may be accompanied by nitrogen and air, etc. and continuously fed to the reaction system or dissolved in a reaction solvent and dropped with time. The molar amount of the nitrogen dioxide to be used is 2-100 times, preferably 5-50 times of that of the aromatic iodine compound.
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公开(公告)号:JPS58110523A
公开(公告)日:1983-07-01
申请号:JP22309082
申请日:1982-12-21
Applicant: BAYER AG
Inventor: ARUBUREHITO MARUHORUTO , EERITSUHI KURAUKE
IPC: C07C41/30 , C07B31/00 , C07B37/00 , C07C17/00 , C07C17/14 , C07C17/20 , C07C17/26 , C07C17/263 , C07C22/08 , C07C25/02 , C07C25/13 , C07C27/00 , C07C37/11 , C07C37/18 , C07C41/00 , C07C43/02 , C07C43/225 , C07C43/23 , C07C67/00 , C07C201/00 , C07C201/10 , C07C205/11 , C07C313/00 , C07C319/20 , C07C323/07 , C07D317/46 , C07D319/20
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公开(公告)号:JPWO2017195619A1
公开(公告)日:2019-03-14
申请号:JP2017016700
申请日:2017-04-27
Applicant: クミアイ化学工業株式会社
IPC: C07C205/12 , C07C205/58 , C07C201/10
Abstract: 本発明の目的は、経済的に好ましくかつ工業化に適した、下記一般式(1)のニトロベンゼン化合物の製造方法を提供することにある。 本発明は、次の一般式(1): (式中、R 1 はハロゲン原子を示し;R 2 、R 3 及びR 4 は水素原子等を示し;R 5 はハロゲン原子又はアルコキシカルボニル基を示す。) のニトロベンゼン化合物の製造方法であって、以下の工程: (i) 一般式(2): (式中、R 1 、R 2 、R 3 、R 4 及びR 5 は前記で定義した通りである。) のアニリン化合物を亜硝酸の金属塩と硝酸の存在下で反応させる工程; (ii) 工程(i)の生成物を亜硝酸の金属塩と銅化合物の存在下で反応させる工程、 を含む方法に関する。
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公开(公告)号:JP2013534212A
公开(公告)日:2013-09-02
申请号:JP2013519864
申请日:2011-07-15
Applicant: アッヴィ・インコーポレイテッド
Inventor: シエカール,シヤシヤンク , フランチエク,サデイアス・エス , バーンズ,デイビツド・エム , ダン,トラビス・ビー , へイト,アンソニー・アール , チヤン,ビンセント・エス
IPC: C07F9/6568 , B01J31/04 , B01J31/24 , B01J31/26 , C07B39/00 , C07B61/00 , C07C1/26 , C07C15/06 , C07C17/093 , C07C25/13 , C07C41/16 , C07C43/205 , C07C45/65 , C07C45/68 , C07C49/784 , C07C201/10 , C07C205/45 , C07C253/30 , C07C255/50 , C07C273/18 , C07C275/28 , C07C303/36 , C07C311/08 , C07C319/14 , C07C321/30 , C07F5/04 , C07F9/40 , C07F9/6571
CPC classification number: C07F9/657163 , B01J31/189 , B01J31/2423 , B01J31/2466 , B01J31/2485 , B01J31/249 , B01J2231/344 , B01J2231/4227 , B01J2231/4283 , B01J2231/4288 , B01J2231/4294 , B01J2531/0205 , B01J2531/0266 , B01J2531/0288 , B01J2531/824 , B01J2540/10 , B01J2540/40 , C07C1/30 , C07C1/321 , C07C15/14 , C07C17/093 , C07C17/361 , C07C41/09 , C07C45/68 , C07C201/10 , C07C253/30 , C07C273/1854 , C07C273/1863 , C07C303/40 , C07C315/04 , C07C319/14 , C07C319/18 , C07C2523/42 , C07C2523/44 , C07C2523/46 , C07C2523/52 , C07C2523/72 , C07C2523/75 , C07C2523/755 , C07C2527/14 , C07C2531/22 , C07C2531/24 , C07D209/34 , C07D239/54 , C07D295/033 , C07F5/027 , C07F9/40 , C07F9/65036 , C07F9/65515 , C07F9/6552 , C07F9/65683 , C07F9/6571 , C07F9/6584 , Y02P20/52 , C07C275/28 , C07C311/08 , C07C311/21 , C07C311/29 , C07C255/10 , C07C321/30 , C07C205/45 , C07C15/06 , C07C49/784 , C07C25/18
Abstract: 本発明は(a)ホスファサイクルリガンド;(b)結合形成反応における前記ホスファサイクルリガンドの使用方法;及び(c)ホスファサイクルリガンドの製造方法に関する。
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公开(公告)号:JP2011507941A
公开(公告)日:2011-03-10
申请号:JP2010540175
申请日:2008-12-19
Applicant: ジェネリクス・(ユーケー)・リミテッド , マイラン・デベロップメント・センター・プライベート・リミテッド
Inventor: アブヘイ・ガイトンデ , スナンダ・パドタール , デバシシュ・ダッタ , ビンドゥ・マノジュクマール
IPC: C07C227/06 , A61K31/195 , A61P9/10 , A61P21/00 , A61P25/04 , A61P25/08 , A61P25/18 , A61P25/22 , A61P25/24 , C07B61/00 , C07C67/307 , C07C67/31 , C07C69/24 , C07C69/675 , C07C201/10 , C07C201/12 , C07C205/51 , C07C227/34 , C07C229/08 , C07C303/28 , C07C309/70 , C12P7/40
CPC classification number: C07C227/32 , C07B2200/07 , C07C67/307 , C07C67/31 , C07C67/343 , C07C201/12 , C07C227/04 , C07C229/08 , C07C309/65 , C12P7/42 , C12P41/002 , C07C69/63 , C07C69/675 , C07C69/716 , C07C205/51
Abstract: The present invention relates to a novel method for the preparation of racemic pregabalin (1) or a single enantiomer thereof, (S)-(+)-3-(aminomethyl)-5-methyl-hexanoic acid (2).
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公开(公告)号:JP2007522253A
公开(公告)日:2007-08-09
申请号:JP2006553511
申请日:2005-02-15
Inventor: ルーロフ コルネリウス , レープベッケ シュテファン , ボスコヴィッチ ドゥサン , テュルケ トビアス , アンテス ユルゲン , ハーゼ ユルゲン
IPC: C07C201/10 , B01J19/00 , C07C201/02 , C07C203/04 , C07C203/06
CPC classification number: C07C201/02 , B01J19/0093 , B01J2219/00822 , B01J2219/00824 , B01J2219/00826 , B01J2219/00831 , B01J2219/0086 , B01J2219/00889 , C07C203/06
Abstract: 硝酸を用いてアルコールをエステル化し、その際、反応を1つまたは複数のマイクロリアクター中で実施する、液体の硝酸エステル、例えばニトログリセリンの製造法を記載する。
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