HALOGENATION OF UNSATURATED ESTERS-II. ADDITION OF Cl2, BrCl AND Br2 TO METHYL ESTERS OF MONOCHLOROPROPENOIC ACIDS

DOI: 10.1016/S0040-4020(01)91588-1

Source and publish data:

Tetrahedron p. 3367 - 3372 (1983)

Update date:2022-08-03

Topics:

Authors:

Pitkaenen, Maija

Korhonen, Ilpo O. O.

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1016/S0040-4020(01)91588-1

The addition of chlorine, bromine chloride and bromine to methyl 2-chloropropenoate 1, methyl cis-3-chloropropenoate 2 and methyl trans-3-chloropropenoate 3 under ionic and radical conditions gave regioisomer mixtures.Both trans- and cis-addition of halogen species was observed, bromine preferentially adding to the non-halogenated carbon atom.

Full text of DOI:10.1016/S0040-4020(01)91588-1

Products guided by the article

Product name:Propanoic acid, 3-bromo-2,2-dichloro-, methyl ester

Cas No:89294-73-5

R&D Labs maybe for 89294-73-5

Zhejiang Kaili Industrial Co., Ltd

Contact:+86-571-85241926

Address:lantian business center,No.18 Moganshan Road
Borun Chemical Co.,Ltd.

Contact:+86-574- 87178138; 87297407

Address:No. 809, Liudingxingzuo, cangsong road, Ningbo, China
Foreschem Co., Ltd

Contact:+86-533-3112891

Address:zibo
Li's chemicals

Contact:+86-15850770348

Address:51 OF XIANGFANGCUN ROAD, Nanjing 210002, China
Anhui Asahikasei Chemical Co., Ltd

Contact:86-551-4259770

Address:No. 88 Linquan Road Hefei Anhui China

Relevant to this article

Organic catalysis of phospha-aldol condensation

Doi:10.1134/S1070363208110091
(2008)
1-arylsulfonyl-3-(α-hydroxybenzyl)-1H-pyrroles, a novel class of anti-HIV-1 reverse transcriptase inhibitors

Doi:10.1016/S0960-894X(97)00340-5
(1997)
A PRACTICAL METHOD FOR MULTIGRAM SCALE SYNTHESIS OF (+)-METHYL 5(S),6(R)-EPOXY-6-FORMYLHEXANOATE AND 2(R),3(S)-EPOXYOCTANAL, KEY INTERMEDIATES FOR SYNTHESIS OF LEUKOTRIENES A₄

Doi:10.1016/S0040-4039(00)85062-5
(1986)
Doi:10.1021/ja01509a031
(1960)
Design of chimeric histone deacetylase- and tyrosine kinase-inhibitors: A series of Imatinib hybrides as potent Inhibitors of wild-type and mutant BCR-ABL, PDGF-Rβ, and histone deacetylases

Doi:10.1021/jm800988r
(2009)
Structural studies on octahedral diorganotin(IV) complexes: the influence of substituents in carbon- and heteroatom-donor ligands on skeletal geometry

Doi:10.1016/S0022-328X(00)99748-1
(1987)

Article Doi