Preparation of α-substituted acroleins via the reaction of aldehyde with dihalomethane and diethylamine
YS Hon, FJ Chang, L Lu
Index: Hon, Yung-Son; Chang, Feng-Jon; Lu, Ling Journal of the Chemical Society, Chemical Communications, 1994 , # 18 p. 2041 - 2042
Full Text: HTML
Citation Number: 6
Abstract
Treatment of ozonides or aldehydes with a mixture of dihalomethane and diethylamine in dichloromethane affords α-substituted acroleins in good yields, the β-carbon of the acrolein being derived from dihalomethane; the relative rates and yields are in the following order: CH2l2> CH2Br2> CH2Cl2.
Related Articles:
[Hon, Yung-Son; Chang, Feng-Jon; Lu, Ling; Lin, Wei-Chi Tetrahedron, 1998 , vol. 54, # 20 p. 5233 - 5246]
[Harada, Hiroshi; Morie, Toshiya; Hirokawa, Yoshimi; Kato, Shiro Chemical and Pharmaceutical Bulletin, 1996 , vol. 44, # 12 p. 2205 - 2212]
[Harada, Hiroshi; Morie, Toshiya; Hirokawa, Yoshimi; Kato, Shiro Chemical and Pharmaceutical Bulletin, 1996 , vol. 44, # 12 p. 2205 - 2212]