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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1730747Generated: October 31, 2026

Chloroform → HCID 53703941, compound

https://huagongshe.com/reaction/1730747

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantMethyl iodideHCID 6328—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 20348737HCID 20348737—
CatalystTetrabutylammonium IodideHCID 67553—
SolventWaterHCID 962—
ProductHCID 53703941HCID 53703941—

Reaction Steps

1.1 gm (3 millimols) of tetrabutylammonium iodide and 3.06 gm (10 millimols) of [1-(2'-fluoro-4-biphenylyl)-ethylsulfinyl]-acetic acid (m.p. 164° - 165° C) were added to a solution of 730 mgm (13 millimols) of potassium hydroxide in 20 ml of water, then 20 ml of chloroform and 2 ml of methyl iodide were added, and the mixture was stirred at room temperature for 10 hours. Afterwards, the organic phase was separated from the neutral aqueous phase, washed with dilute hydrochloric acid and then with water, dried and evaporated. The residue (3.6 gm) was purified by chromatography on 100 gm of silicagel (grain size: 0.05 - 0.2 mm) with cyclohexane ethyl acetate = 1/4. After evaporation of the combined fractions with an Rf -value of 0.4 and recrystallization of the residue from isopropanol, 1.7 gm (53% of theory) of the title compound m.p. 75° - 77° C were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03993683
Source datasetuspto-grants-1976_11
ORD IDord-ce0772d0b453474390f69ca151360bfe
Source noteuspto-grants-1976_11