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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 848749Generated: October 28, 2026

Pyridine → alpha-Chloro-alpha-(2,4-dichlorophenyl)-acetic acid t-butyl ester

https://huagongshe.com/reaction/848749

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactanttert-ButanolHCID 6386—
Reactantalpha-Chloro-alpha-(2,4-dichlorophenyl)-acetyl chlorideHCID 20564372—
SolventDichloromethaneHCID 6344—
Productalpha-Chloro-alpha-(2,4-dichlorophenyl)-acetic acid t-butyl esterHCID 5419123082.6%

Reaction Steps

While stirring and with ice cooling, a solution of 17.6 g of t-butanol and 19.2 ml of pyridine in 60 ml of dichloromethane is dripped into a solution, cooled at 5° C., of 62 g of α-chloro-α-(2,4-dichlorophenyl)-acetyl chloride in 60 ml of dichloromethane in such a manner that the temperature of the reaction mixture stays below 10° C. After all the solution has been dripped in, the mixture is stirred overnight at room temperature, is then diluted with 100 ml of dichloromethane and extracted 5 times, each time with 100 ml of water. The organic phase is dried over magnesium sulfate and distilled after the solvent has been evaporated. There is obtained 58 g of α-chloro-α-(2,4-dichlorophenyl)-acetic acid t-butyl ester as a colorless oil; b.p. 98°-103° C./0.13 mbar.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04297364
Source datasetuspto-grants-1981_10
ORD IDord-f400aa52fe434e649fda6c635634b4cc
Source noteuspto-grants-1981_10