1,3-二甲氧基乙酮置于对甲苯磺酸体系中,用 苯 作为反应溶剂,化学反应 24.0H,以62%的收率获得产物1,1-二甲氧基丙酮 参考文献:Yu,Yin; Chen,Guo-Qiang; Zhu,Jun,Journal Of The Chemical Society. Perkin Transactions I,1990,# 8,P. 2239-2243 标题:Yu,Yin; Chen,Guo-Qiang; Zhu,Jun,Journal Of The Chemical Society. Perkin Transactions I,1990,# 8,P. 2239-2243
专利号:WO-2025053792-A1 优先权日:2023-09-06 标题:Collective synthesis of phantomolin family through total synthesis of the sesquiterpene lactone molephantin 发明人:CHIBA SHUNSUKE; PATOURET REMI HENRI LOUIS; LI HOI YEUNG; LAI SOAK KUAN 权利人:UNIV NANYANG TECH 摘要:Disclosed herein are processes to generate an intermediate in the total synthesis of (+)- molephantin or a derivative thereof, and a total synthesis of (+)-molephantin or a derivative thereof. Also disclosed herein are methods of forming a compound of formula XIV and of forming a compound of formula XV, wherein compound of formula XIV and compound of formula XV are as defined in the description.
专利号:US-7884128-B2 优先权日:2005-10-13 标题:Process for total synthesis of pladienolide B and pladienolide D 发明人:KANADA REGINA MIKIE; ITO DAISUKE; SAKAI TAKASHI; ASAI NAOKI; KOTAKE YOSHIHIKO; NIIJIMA JUN 权利人:EISAI R&D MAN CO LTD 摘要:Process for producing compound of Formula: n nwherein P 2 , P 3 and R 2 are the same as defined below, characterized by comprising reacting a compound represented by Formula (7):n n nwherein P 3 means a protecting group for hydroxy group; and Het means a 1-phenyl-1H-tetrazol-5-yl group, with a compound represented by Formula (8):n n nwherein P 2 means a protecting group for hydroxy group; and R 2 means a phenyl group which may be substituted, in the presence of a base.
专利号:US-9187394-B2 优先权日:2011-12-26 标题:Method for synthesizing 2,7-dimethyl-2,4,6-octatriene-1,8-dialdehyde 发明人:LV CHUNLEI; PI SHIQING; CHEN JIANHUI; LU DINGQIANG; OUYANG PINGKAI 权利人:NANJING UNIVERSITY OF TECHNOLOGY; ZHEJIANG MED XINCHANG PHARM 摘要:Provided in the present invention is a method for synthesizing 2,7-dimethyl-2,4,6-octatriene-1,8-dialdehyde. The synthesis method comprises the following steps: (1) adding acetaldehyde diethyl acetal and ethyl-(1-propenyl)-ether under the effect of a catalyst to produce 1,1,3-triethoxy-2-methyl-butane; (2) pyrolysis synthesizing 1,1,3-triethoxy-2-methyl-butane under the catalytic effects of isoquinoline and p-Toluenesulfonic acid to produce 1-methoxy-2-methyl-1,3-butadiene; (3) dissolving 1-methoxy-2-methyl-1,3-butadiene in anhydrous ethanol solvent for synthesis with a phase transfer catalyst, cetyl-trimethyl ammonium bromide, and a chlorinating agent, trichloroisocyanuric acid, to generate 4,4-diethoxy-3-methyl-1-chloro-butene; (4) combining 4,4-diethoxy-3-methyl-1-chloro-butene with a triphenylphosphine salt to produce a phosphonium salt; and (5) condensing the phosphonium salt under the effects of hydrogen peroxide in conjunction with sodium carbonate solution to generate 1,1,8,8-tetramethyl-2,7-dimethyl-2,4,6-octatriene; then hydrolyzing under acidic conditions to synthesize 2,7-dimethyl-2,4,6-octatriene-1,8-dialdehyde. The present invention has a simple process route, is easy to operate, and has mild conditions, great yield, and great industrial value.
专利号:US-2008021226-A1 优先权日:2005-10-13 标题:Process for total synthesis of pladienolide B and pladienolide D
专利号:US-2010204490-A1 优先权日:2005-10-13 标题 :Process for total synthesis of pladienolide b and pladienolide d
专利号:EP-0122479-A1 优先权日:1983-03-18 标 题:3-Chloro-1,1-dialkoxy-acetones and process for their preparation 发明人:PETERSEN HERMANN DR DIPL-CHEM; DEINHAMMER WOLFGANG DR DIPL-IN 权利人:WACKER CHEMIE GMBH 摘要:The invention relates to 3-chloro-1, 1-dialkoxy-acetones of the formula where R is alkyl radicals having 1 to 5 carbon atoms, which, because of their functional groups, are valuable intermediates, in particular for the synthesis of folic acid derivatives. These compounds can be obtained by reacting mixtures of 3-chloro-1-hydroxyimino-acetone and an alkanol with alkyl nitrites in the presence of an inorganic electron pair acceptor, such as hydrogen chloride, at temperatures in the range from -25 ° C to + 60 ° C and purification of the crude products thus obtained by distillation under reduced pressure. 3-Chloro-1-hydroxyiminoacetone, which was obtained immediately before use by reacting 4-chloroacetoacetic acid with sodium nitrite in aqueous solution and subsequent extraction with an organic solvent, as well as alkanols and alkyl nitrites, each having identical alkyl radicals, can be used as reactants Contain 1 to 5 carbon atoms can be used. The compounds that can be produced in this way are stable at room temperature and can be stored for a long time without any tendency to decompose.
[参考文献]: Ricardo A Gomes, Et Al. Protein Glycation In Saccharomyces Cerevisiae. Argpyrimidine Formation And Methylglyoxal Catabolism. Febs J. 2005 Sep;272(17):4521-31.
合成参考文献
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