Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701166Generated: October 29, 2026

Chloroform → HCID 53703941, compound

https://huagongshe.com/reaction/1701166

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 numberUS04191776
Source datasetuspto-grants-1980_03
ORD IDord-5b279a8695ed460f8018d6edb9b30545
Source noteuspto-grants-1980_03