合成目标产物 Paraldehyde 主要起始原料 Ethanol And Acetaldehyde
(文献来源)合成步骤主要原料 Ethanol 和 Acetaldehyde
Ethyl Hypochlorite置于乙醇体系中,化学反应生成三聚乙醛 参考文献:Chattaway; Backeberg,Journal Of The Chemical Society,1924,Vol. 125,P. 1099 标题:Chattaway; Backeberg,Journal Of The Chemical Society,1924,Vol. 125,P. 1099
专利号:WO-2016056031-A1 优先权日:2014-10-08 标题:Novel diol compounds synthesis and its use for formal synthesis of (2r, 3 s)-3-hydroxypipecolic acid 发明人:CHAVAN SUBHASH PRATAPRAO; PAWAR KAILASH PRALHAD 权利人:COUNCIL SCIENT IND RES 摘要:The patent discloses novel diol derivatives of general formula I, [Formula should be inserted here] A chiral pool process for the synthesis of the compound of formula I from D glucose. Further, it discloses a process for the synthesis of (2 R , 3 S )-3-hydroxypipecolic acid from D- glucose using chiral pool approach, wherein the D-glucose used is in enantiomerically pure form.
专利号:US-4592874-A 优先权日:1980-05-14 标 题:Process for the synthesis of alpha-chlorinated chloroformates 发明人:CAGNON GUY C; PITEAU MARC D; SENET JEAN-PIERRE G; OLOFSON ROY A; MARTZ JONATHAN T 权利人:POUDRES & EXPLOSIFS STE NALE 摘要:Process for the synthesis of alpha -chlorinated chloroformates, and new alpha -chlorinated chloroformates. The invention relates to a new process for the manufacture of alpha -chlorinated chloroformates and, to new alpha -chlorinated chloroformates as new industrial products. The process according to the invention consists of a synthesis, by catalytic phosgenation, of alpha -chlorinated chloroformates of the formula: in which: R represents a substituted or unsubstituted hydrocarbon radical and m represents an integer superior or equal to one, this synthesis consisting in reacting phosgene with the aldehyde R-CHO)m, in the presence of a catalyst which is an organic or inorganic substance which is capable in a medium containing an aldehyde of the formula R-CHO)m, phosgene and, possibly, a solvent, of generating a pair of ions one of which is an halogenide anion and the other is a cation which is sufficiently separated from said halogenide anion so as to give to the latter a nucleophilic power enabling it to react with the function(s) aldehyde of the molecule R-CHO)m.
专利号:EP-3263552-A1 优先权日:2016-06-28 标 题:Methods for preparing intermediates for the synthesis of obeticholic acid 发明人:KUBELKA TOMAS; SLAVIKOVA MARKETA; ZEZULA JOSEF; CERNY JOSEF 权利人:ZENTIVA KS 摘要:The present invention discloses a method for preparing the key intermediates of formula 2 (disilylated derivative) and enones of formula 3 (mixture of E/Z isomers) for synthesis of the active pharmaceutical ingredient - obeticholic acid of formula 1. The principle of the method is that it comprises a reaction of the compound of formula 8 , wherein R 1 is a C1 to C4 linear or branched alkyl, with trimethylsilyl iodide in the presence of a base and a mixture of a polar aprotic and non-polar solvent under an inert atmosphere at a temperature in the range of from 40°C to 70°C.
专利号:US-9701634-B2 优先权日:2009-06-24 标 题 :Process for the synthesis of 3-methyl-pyridine 发明人:ROEDERER DETLEF; ZOLLINGER DANIEL; DE RIEDMATTEN JEAN-YVES 权利人:ROEDERER DETLEF; ZOLLINGER DANIEL; DE RIEDMATTEN JEAN-YVES; LONZA AG 摘要:The present invention discloses a process for the synthesis of 3-methyl-pyridine from formaldehyde, paracetaldehyde, ammonia and acetic acid, whereby said compounds are reacted and said process comprises the following parameters:n a) a reaction temperature of 260-300° C.; b) a molar ratio of formaldehyde and paraldehyde (calculated as acetaldehyde) of 0.7-1.4 mol/mol: c) an ammonia concentration of 10-20 weight-% d) an acetic acid concentration of 4-20 weight-% e) a paraldehyde (calculated as acetaldehyde) concentration of 0.4-1.6 Mol/kg f) a retention time of 10-30 minutes in case of a continuous reaction and 10-90 minutes in case of a discontinuous reaction; and g) a reaction pressure of 30-130 bar.
专利号:US-10717718-B2 优先权日:2015-11-17 标 题:5-azido-5-deoxy-2 :3-isopropylidene-D-arabinose compounds; their method of manufacture and their use for the synthesis of ARA-N3, KDO-N3 and 4EKDO-N3 发明人:VAUZEILLES BORIS; MAS PONS JORDI; BARON AURÈLIE 权利人:CENTRE NAT RECH SCIENT 摘要:Disclosed are new compounds of formulae: n nWherein: R 1 and R 2 can be independently H; a C 1 to C 6 alkyl including methyl, ethyl, propyl, butyl; aryl including phenyl, para-methoxyphenyl; or R 1 ,R 2 together with the carbon C-6 can be a cyclopentylidene or cyclohexylidene; each of these groups being substituted or not; and R 3 can be a C 1 to C 6 alkyl including methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tert-butyl, pentyl; or aryl including phenyl, methylphenyl, ethylphenyl, each of these groups being substituted or not. The invention also relates to their method of manufacture and their use for the synthesis of Ara-N 3 , Kdo-N 3 and 4eKdo-N 3 .
专利号:US-8309716-B2 优先权日:2005-07-29 标题 :Pyrrolo[2,3-d]pyrimidine derivatives: their intermediates and synthesis 发明人:RUGGERI SALLY GUT; HAWKINS JOEL M; MAKOWSKI TERESA M; RUTHERFORD JENNIFER L; URBAN FRANK J 权利人:RUGGERI SALLY GUT; HAWKINS JOEL M; MAKOWSKI TERESA M; RUTHERFORD JENNIFER L; URBAN FRANK J; PFIZER 摘要:This invention relates to methods and intermediates useful for the synthesis of pyrrolo[2,3-d]pyrimidine compounds. Specifically novel synthetic methods and intermediates for the synthesis of 3-{(3R,4R)-4-methyl-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-amino}-piperidin-1-yl)-3-oxo-propionitrile and its corresponding citrate salt are disclosed.
摘要:Journal of Pharmacology and Experimental Therapeutics., 119(19), 1957 [] 摘要:South African Medical Journal., 29(1021), 1955 摘要:ASHP. American Hospital Formulary Service -Drug Information 87. Bethesda, MD: American Society of Hospital Pharmacists, 1987. (Plus Supplements, 1987), p.) 1172 摘要:Association of American Railroads. Emergency Handling of Hazardous Materials in Surface Transportation. Washington, DC: Association of American Railroads, Bureau of Explosives, 1992., p. 726 摘要:40 CFR 60.489 (7/1/92)