Chemistry of Heterocyclic Compounds p. 161 - 163 (1999)
Update date:2022-08-12
Topics:
Saldabol
Popelis
Shatz
Slavinskaya
The bromination of 2-acetyl-5-methylfuran by bromine and N-bromosuccinimide was studied. The action of N-bromosuccinimide on 5-methyl-2-acetylfuran in various solvents leads to mixtures of an ω-bromo ketone, a 5-bromomethyl derivative, and 5-bromomethyl-ω-bromo ketone. The use of 2,2′-azobisisobutyronitrile as activator of the radical process does not make the reaction selective but promotes bromination at the methyl group of the ring. A selective method for the synthesis of 2-(bromoacetyl)-5-methylfuran by the bromination of 2-acetyl-5-methylfuran with bromine was developed. 1999 KluwerAcademic/Plenum.
View More
Contact:0792-8228321
Address:10TH Floor No.121 binjiang Road Xunyang District
Xi'an Kaixiang Photoelectric Technology Co., Ltd
website:http://www.kxmaterials.com/
Contact:86-29-15991651477
Address:Building 6, Biopharmaceutical Industry R&D Cluster Base, No. 16, Caotang 4th Road, Caotang Science and Technology Industrial Base, High-tech Zone, Xi'an City, Shaanxi Province, China
website:http://www.weichichem.com
Contact:+8613912949432
Address:Fine Chemical Industrial Base,Wujiang town,He County,Anhui China.
hangzhou verychem science and technology co.ltd
website:http://www.verypharm.com
Contact:+86-571-88162785; 88162786
Address:F1502, 753 Shenhua road, Hangzhou, China
ChangZhou XiaQing Chemical Co., Ltd.
Contact:+86-519-88721665
Address:3# Hengluo Road, Henglin Town, Changzhou City, Jiangsu Province，China
Doi:10.1080/00397910600639752
(2006)Doi:10.1016/j.jcat.2008.12.007
(2009)Doi:10.1016/j.bmcl.2015.10.022
(2015)Doi:10.1021/j100511a007
(1978)Doi:10.1016/j.tet.2016.04.042
(2016)Doi:10.1016/S0957-4166(02)00643-2
(2002)
