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公开(公告)号:DK137640C
公开(公告)日:1978-10-09
申请号:DK445575
申请日:1975-10-02
Applicant: HOECHST AG
IPC: C07C20060101 , C07C307/00 , C07C67/00 , C07C301/00 , C07C303/36 , C07D291/06 , C07C143/86
Abstract: 1476101 N-Fluorosulphonylacetoacetamide HOECHST AG 2 Oct 1975 [3 Oct 1974] 40314/75 Heading C2C N-Fluorosulphonylacetoacetamide is prepared by reacting sulphamoyl fluoride with diketene at 50-100 C., preferably in an inert solvent. It may be reacted with methanolic KOH to give 6-methyl-3,4-dihydro-1,2,3- oxathiazine-4-one-2,2-dioxide as the potassium salt.
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公开(公告)号:DK445575A
公开(公告)日:1976-04-04
申请号:DK445575
申请日:1975-10-02
Applicant: HOECHST AG
IPC: C07C20060101 , C07C307/00 , C07C67/00 , C07C301/00 , C07C303/36 , C07D291/06 , C07C
Abstract: 1476101 N-Fluorosulphonylacetoacetamide HOECHST AG 2 Oct 1975 [3 Oct 1974] 40314/75 Heading C2C N-Fluorosulphonylacetoacetamide is prepared by reacting sulphamoyl fluoride with diketene at 50-100 C., preferably in an inert solvent. It may be reacted with methanolic KOH to give 6-methyl-3,4-dihydro-1,2,3- oxathiazine-4-one-2,2-dioxide as the potassium salt.
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公开(公告)号:DK137640B
公开(公告)日:1978-04-10
申请号:DK445575
申请日:1975-10-02
Applicant: HOECHST AG
IPC: C07C20060101 , C07C307/00 , C07C67/00 , C07C301/00 , C07C303/36 , C07D291/06 , C07C143/86
Abstract: 1476101 N-Fluorosulphonylacetoacetamide HOECHST AG 2 Oct 1975 [3 Oct 1974] 40314/75 Heading C2C N-Fluorosulphonylacetoacetamide is prepared by reacting sulphamoyl fluoride with diketene at 50-100 C., preferably in an inert solvent. It may be reacted with methanolic KOH to give 6-methyl-3,4-dihydro-1,2,3- oxathiazine-4-one-2,2-dioxide as the potassium salt.
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公开(公告)号:DK135992C
公开(公告)日:1978-01-02
申请号:DK326575
申请日:1975-07-17
Applicant: HOECHST AG
IPC: A23L27/30 , C07D291/06 , C07D291/08
Abstract: 6-Methyl-3,4-dihydro-1,2,3-oxathiazin-4-one-2,2-dioxide and the nontoxic salts thereof are prepared by reacting acetone and fluorosulfonyl isocyanate in a molar proportion of from 14:1 to 150:1 at a temperature of from 0 DEG to 60 DEG C, distilling off the excess acetone from the reaction mixture with acetoacetamide-N-sulfofluoride and bringing about cyclization by a treatment with bases at a pH of from 5 to 12. The oxathiazinone derivatives are used as sweeteners.
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公开(公告)号:DK326775A
公开(公告)日:1976-01-19
申请号:DK326775
申请日:1975-07-17
Applicant: HOECHST AG
IPC: A23L27/30 , C07D291/06 , C07D
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公开(公告)号:DK135992B
公开(公告)日:1977-07-25
申请号:DK326575
申请日:1975-07-17
Applicant: HOECHST AG
IPC: A23L27/30 , C07D291/06 , C07D291/08
Abstract: 6-Methyl-3,4-dihydro-1,2,3-oxathiazin-4-one-2,2-dioxide and the nontoxic salts thereof are prepared by reacting acetone and fluorosulfonyl isocyanate in a molar proportion of from 14:1 to 150:1 at a temperature of from 0 DEG to 60 DEG C, distilling off the excess acetone from the reaction mixture with acetoacetamide-N-sulfofluoride and bringing about cyclization by a treatment with bases at a pH of from 5 to 12. The oxathiazinone derivatives are used as sweeteners.
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公开(公告)号:DK326975A
公开(公告)日:1976-01-19
申请号:DK326975
申请日:1975-07-17
Applicant: HOECHST AG
IPC: C07C307/00 , C07C67/00 , C07C301/00 , C07C303/00 , C07D205/08 , C07D291/06 , C07C
Abstract: Compounds of the formula +q,10 IN WHICH R represents an alkyl radical having from 1 to 4 carbon atoms and Hal stands for fluorine or chlorine are prepared by reacting at a temperature of from -40 DEG to +20 DEG C an i-propenylalkanoic acid ester of the formula CH ¦ R-C(O)-O-C=CH2 (IV) with an isocyanate of the formula O=C=N-SO2Hal(V) in which R and Hal have the same meaning as above, and isolating the compound of formula III.
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公开(公告)号:DK326875A
公开(公告)日:1976-01-19
申请号:DK326875
申请日:1975-07-17
Applicant: HOECHST AG
IPC: A23L27/30 , C07D291/06 , C07D291/08 , C07D
Abstract: The potassium salt practically free of fluoride of 6-methyl-3,4-dihydro-1,2,3-oxathiazin-4-one-2,2-dioxide is prepared by cyclization of acetoacetamide-N-sulfofluoride with at least two moles potassium hydroxide, potassium methylate or a mixture of potassium hydroxide and potassium methylate per mole of sulfofluoride in methanol as solvent containing less than 50 % by weight of water at a temperature of from -20 DEG to +60 DEG C and separating the crystalline potassium salt of the oxathiazinone dioxide from the reaction solution. The compound obtained has a pure sweet taste.
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公开(公告)号:DK326675A
公开(公告)日:1976-01-19
申请号:DK326675
申请日:1975-07-17
Applicant: HOECHST AG
IPC: A23L27/30 , C07D265/06 , C07D
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公开(公告)号:DK326575A
公开(公告)日:1976-01-19
申请号:DK326575
申请日:1975-07-17
Applicant: HOECHST AG
IPC: A23L27/30 , C07D291/06 , C07D291/08 , C07D
Abstract: 6-Methyl-3,4-dihydro-1,2,3-oxathiazin-4-one-2,2-dioxide and the nontoxic salts thereof are prepared by reacting acetone and fluorosulfonyl isocyanate in a molar proportion of from 14:1 to 150:1 at a temperature of from 0 DEG to 60 DEG C, distilling off the excess acetone from the reaction mixture with acetoacetamide-N-sulfofluoride and bringing about cyclization by a treatment with bases at a pH of from 5 to 12. The oxathiazinone derivatives are used as sweeteners.
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