Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 487083Generated: October 30, 2026

Methanethiol → HCID 14820158, compound

https://huagongshe.com/reaction/487083

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanethiolHCID 878—
ReactantTriethylamineHCID 8471—
ReactantHCID 14820169HCID 14820169—
SolventDichloromethaneHCID 6344—
ProductHCID 14820158HCID 14820158—

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 600 mg of the compound from Example 127 was dissolved in 50 ml of methylene chloride and cooled to 0° C. Fifteen grams of methanethiol were added followed by the addition of 2 ml of triethylamine. The reaction was allowed to warm to room temperature and was stirred overnight. The reaction mixture was concentrated in vacuo and partitioned between ethyl acetate and an acidic sodium choride solution. The organic layer was separated, dried over sodium sulfate, and concentrated in vacuo. The residue was purified by preparative thin layer chromatography over silica gel eluting with 40% ethyl acetate in hexane providing 200 mg of the desired title product, m.p.=78° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05294613
Source datasetuspto-grants-1994_03
ORD IDord-4d5a69095e2847bb869267345f0901d3
Source noteuspto-grants-1994_03