HYDRATION OF ALKYNES IN ANHYDROUS MEDIUM WITH FORMIC-ACID AS WATER DONOR

被引:63
作者
MENASHE, N [1 ]
SHVO, Y [1 ]
机构
[1] TEL AVIV UNIV,RAYMOND & BEVERLY SACKLER SCH EXACT SCI,SCH CHEM,IL-69978 TEL AVIV,ISRAEL
关键词
D O I
10.1021/jo00078a023
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Formic acid has been found to hydrate alkynes in the absence of water to give oxo products and carbon monoxide. The scope of the reaction of alkynes and formic acid has been delineated. Hydrocarbon alkynes were found to be reactive in the absence of catalyst. Functionalized alkynes, in particular oxygenated alkynes, are inert toward formic acid but can be activated catalytically with Ru3(CO)12. Consequently, all the tested types of alkynes were found to give oxo products and CO with formic acid. The mechanism of the reaction was examined. With some alkynes, the primary oxo products underwent secondary reactions that gave rise to unexpected products.
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页码:7434 / 7439
页数:6
相关论文
共 21 条
[1]  
ARODEE C, 1984, AUST J CHEM, V37, P1255
[2]   ALKYNE HYDRATION PROMOTED BY RHCL3 AND QUATERNARY AMMONIUM-SALTS [J].
BLUM, J ;
HUMINER, H ;
ALPER, H .
JOURNAL OF MOLECULAR CATALYSIS, 1992, 75 (02) :153-160
[3]   SYNTHESIS OF ARYL-SUBSTITUTED AND VINYL-SUBSTITUTED ACETYLENE DERIVATIVES BY USE OF NICKEL AND PALLADIUM COMPLEXES [J].
CASSAR, L .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1975, 93 (02) :253-257
[4]   NATURAL SOURCE OF 3-PHENYLISOCUMARINE [J].
CHARUBALA, R ;
GUGGISBERG, A ;
HESSE, M ;
SCHMID, H .
HELVETICA CHIMICA ACTA, 1974, 57 (04) :1096-1097
[5]  
CONIA JM, 1975, SYNTHESIS-STUTTGART, P1
[6]   PHYSICAL PROPERTIES AND CHEMICAL CONSTITUTION .29. ACETYLENIC COMPOUNDS [J].
GRZESKOWIAK, R ;
JEFFERY, GH ;
VOGEL, AI .
JOURNAL OF THE CHEMICAL SOCIETY, 1960, (DEC) :4719-4722
[7]  
Hoogzand C., 1968, ORGANIC SYNTHESIS VI, V1, P343
[8]  
KAGDOS J, 1983, J ORG CHEM, V48, P1096
[9]  
MARCH J, 1985, ADV ORGANIC CHEM
[10]  
MATOSYAN SG, 1958, ISVEST AKAD NAUK ARM, V11, P421