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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1732633Generated: October 30, 2026

Pyridine → 2,2-Dimethyl-3-(1-bromo-2,2-dichloro-2-bromoethyl)-cyclopropanecarboxylic acid-3-(phenoxy)-alpha-vinyl-benzyl ester

https://huagongshe.com/reaction/1732633

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2,2-Dimethyl-3-(1-bromo-2,2-dichloro-2-bromoethyl)-cyclopropanecarboxylic acid chlorideHCID 12874346—
Reactant1-(3-Phenoxyphenyl)prop-2-en-1-olHCID 12961393—
SolventBenzeneHCID 241—
Product2,2-Dimethyl-3-(1-bromo-2,2-dichloro-2-bromoethyl)-cyclopropanecarboxylic acid-3-(phenoxy)-alpha-vinyl-benzyl esterHCID 20562155—

Reaction Steps

3.2 g of pyridine in 10 ml of benzene is added dropwise at 5° C., with stirring, to 8 g of 3-phenoxy-α-vinyl-benzyl alcohol in 30 ml of benzene. After the addition of 14 g of 2,2-dimethyl-3-(1-bromo-2,2-dichloro-2-bromoethyl)-cyclopropanecarboxylic acid chloride at 10° C., the mixture is stirred for 2 hours at room temperature, and is allowed to stand for a further 10 hours at this temperature. The reaction mixture is diluted with ice water; the organic layer is extracted three times with 100 ml of 3% HCl each time, and subsequently three times with 100 ml of 3% sodium bicarbonate each time; the organic phase is dried with sodium sulfate, and the benzene is distilled off. There is obtained the compound of the formula ##STR9## as colourless oil having a refractive index of nD40° =1.5776. In an analogous manner is also obtained the compound of the formula ##STR10##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04238504
Source datasetuspto-grants-1980_12
ORD IDord-f2280a23d852409894e458af8bd1af50
Source noteuspto-grants-1980_12