Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1973172Generated: October 30, 2026

Methanethiol → HCID 22768209, compound

https://huagongshe.com/reaction/1973172

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanethiolHCID 878—
ReactantSodium HydroxideHCID 14798—
Reactant5-Chloro-2-nitrobenzotrifluorideHCID 67052—
SolventEthanolHCID 702—
ProductHCID 22768209HCID 22768209—

Reaction Steps

The sodium salt of methanethiol is formed by stirring a solution of methanethiol (100 g, 2.0 mole plus a slight excess), sodium hydroxide (80 g, 2.0 mole) and ethanol (2 l.) under nitrogen at 0°-5° C. for 1 hour. To this solution is rapidly added 5-chloro-2-nitrobenzotrifluoride (451.2 g, 2.0 mole). The solution is allowed to warm to room temperature overnight and then refluxed four hours, cooled, filtered and the solvent evaporated off under reduced pressure. The resulting oil is poured into cold water (1 l.), extracted with methylene chloride, dried over magnesium sulfate and the solvent evaporated under reduced pressure to afford a yellow solid. Recrystallization from hexane affords a product having a melting point of 47°-50° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03996277
Source datasetuspto-grants-1976_12
ORD IDord-febcfe2a95be420ab76242d297ff30b9
Source noteuspto-grants-1976_12