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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354703Generated: October 26, 2026

2-Bromopropane → Ethyl alpha-fluoro-alpha-isopropyl-4-chlorophenylacetate

https://huagongshe.com/reaction/354703

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopropaneHCID 6358—
ReactantHexamethylphosphoramideHCID 12679—
ReactantSodium hydrideHCID 24758—
ReactantEthyl alpha-fluoro-4-chlorophenylacetateHCID 13194587—
SolventBenzeneHCID 241—
ProductEthyl alpha-fluoro-alpha-isopropyl-4-chlorophenylacetateHCID 1319458862%

Reaction Conditions

Temperature35 °C

Reaction Steps

A mixture of ethyl α-fluoro-4-chlorophenylacetate (2.3 g), isopropyl bromide (1.10 g), sodium hydride (0.56 g of a 50% mixture in oil), dry hexamethylphosphoramide (6 ml) and dry benzene (6 ml) was heated with stirring at a temperature of 35° C. under nitrogen for a period of 22 hours. The reaction mixture was poured into ice-water and the aqueous mixture extracted with methylene chloride. The methylene chloride extract was dried over anhydrous sodium sulfate and solvent removed by distillation under reduced pressure. The product was chromatographed over silica gel using 15% ethylene dichloride in petroleum ether as eluant to give ethyl α-fluoro-α-isopropyl-4-chlorophenylacetate (1.42 g; 62%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04376784
Source datasetuspto-grants-1983_03
ORD IDord-646e20de2fd34f059facbd8be7296bb3
Source noteuspto-grants-1983_03