Process for producing optically active 3, 7-dimethyl-6-octenol and process for producing intermediate therefor
申请人:——
公开号:US20020004620A1
公开(公告)日:2002-01-10
Provided is citronellol, which has an elegant rosy fragrance and is extremely useful for fragrance impartation to aromatic articles. A mixture of an alkylamine and isoprene in a molar ratio of from 1:4 to 1:4.5 is subjected to telomerization at 80 to 100° C. for 2.5 to 3.5 hours in the presence of an alkyllithium catalyst and/or phenyllithium catalyst to obtain a nerylamine compound containing 2 to 10 wt % &agr;-nerylamine compound represented by general formula (4).
1
From this nerylamine compound, citronellol containing 2 to 10 wt % optically active 3,7-dimethyl-7-octenol is produced through the reaction steps of asymmetric isomerization, hydrolysis, and hydrogenation.
Process for producing optically active 3,7-dimethyl-6-octenol and process for producing intermediate therefor
申请人:TAKASAGO INTERNATIONAL CORPORATION
公开号:US20020128525A1
公开(公告)日:2002-09-12
Provided is citronellol, which has an elegant rosy fragrance and is extremely useful for fragrance impartation to aromatic articles A mixture of an alkylamine and isoprene in a molar ratio of from 1:4 to 1:4.5 is subjected to telomerization at 80 to 100° C. for 2.5 to 3.5 hours in the presence of an alkyllithium catalyst and/or phenyllithium catalyst to obtain a nerylamine compound containing 2 to 10 wt % &agr;-nerylamine compound represented by general formula (4).
1
From this nerylamine compound, citronellol containing 2 to 10 wt % optically active 3,7-dimethyl-7-octenol is produced through the reaction steps of asymmetric isomerization, hydrolysis, and hydrogenation.
Palladium(II)–acetylacetonate complexes containing phosphine and diphosphine ligands and their catalytic activities in telomerization of 1,3-dienes with diethylamine
作者:Dmitry S. Suslov、Mikhail V. Bykov、Marina V. Belova、Pavel A. Abramov、Vitaly S. Tkach
DOI:10.1016/j.jorganchem.2013.11.017
日期:2014.2
A series of novel [Pd(acac-O,O')((PP)-P-boolean AND)] BF4 and known complexes [Pd(acac-O,O')(PR3)(2)]BF4 ((PP)-P-boolean AND = dppm (1), dppp (2), dppb (3), dppf (4); R = Ph (5), p-Tol (6), i-Pr (7); acac = 2,4-pentanedionato) were prepared by the reaction of [Pd(acac-O,O')(MeCN)(2)]BF4 (1) with appropriate ligands. Complex 2 was characterized by single-crystal X-ray analysis. Models of the structure and IR wavenumbers assignments of the cations of 1-4 were obtained by DFT calculations. Synthesized complexes were tested as catalysts in the telomerization of isoprene and butadiene with diethylamine. In the case of telomerization of butadiene with diethylamine high catalyst activity (e. g. TOFav = 1940 h(-1) and TON up to 17,480 for complex 5) was obtained. (C) 2013 Elsevier B. V. All rights reserved.
Process for producing optically active 3,7-dimethyl-6-octenol and process for producing intermediate therefore