
Journal of the Chemical Society. Perkin transactions I p. 2608 - 2614 (1981)
Update date:2022-09-26
Topics:
Cambie, Richard C.
Hayward, Rodney C.
Jurlina, Jeffrey L.
Rutledge, Peter S.
Woodgate, Paul D.
Treatment of a thallium(I) carboxylate with 1 molar equivalent of bromine gives the corresponding thallium(III) carboxylate dibromide.High yields of primary alkyl bromides are obtained if the thallium(III) carboxylate dibromide is treated with 0.5 mol equiv. of bromine in refluxing carbon tetrachloride.Pyrolysis of the thallium(III) derivative in the absence of added bromine gives a low yield of the corresponding alkyl bromide.The use of thallium(I) carboxylates for the preparation of alkyl bromides in high yields is limited to the salts of primary carboxylic acids.A simple procedure for the preparation of alkyl bromides from carboxylic acids using thallium(I) carbonate has been developed.
View Morewebsite:https://www.sinoshiny.com/products
Contact:+86-20-62802632;62802633
Address:Room 330 GIGCAS Building,No.511 Kehua Street,Tianhe District
Contact:+86-20-32051076
Address:1105,Building A, International Business Incubator,Science City
Jiangxi Global Natural Spice Co., Ltd.
website:https://www.jxhqxl.com/
Contact:+86-796-8106598
Address:No.89, Wenshan Road,South Industrial Park, Jishui County,Jiangxi Province
Jinan Jinguilin Chemical Co.,Ltd
Contact:+86-531-81188412
Address:3rd floor of Torch Building, Huanyuan Rd, City of Jinan
Zhejiang Golden-Shell Pharmaceutical Co.,Ltd.
Contact:+86-576-87501888 / 87501988
Address:No.89 Zhongxing Road. Li'ao, Yuhuan, Zhejiang, China
Doi:10.1016/S0040-4039(01)00229-5
(2001)Doi:10.1016/S0957-4166(00)00498-5
(2001)Doi:10.1139/v71-525
(1971)Doi:10.1002/ejoc.202000771
(2020)Doi:10.1016/0040-4039(80)80225-5
(1980)Doi:10.1039/c39770000602
(1977)