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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 636253Generated: October 30, 2026

Hydrogen Sulfide → 4′-Methyl[1,1′-biphenyl]-2-carbothioamide

https://huagongshe.com/reaction/636253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen SulfideHCID 402—
Reactant2-Cyano-4'-methylbiphenylHCID 145512—
SolventMethanolHCID 887—
SolventTriethylamineHCID 8471—
Product4′-Methyl[1,1′-biphenyl]-2-carbothioamideHCID 21711274—

Reaction Steps

First, 2.00 g of 2-cyano4′-methyl-1,1′-biphenyl was dissolved in a mixture of 15 ml of methanol and 4.18 g of triethylamine, and hydrogen sulfide gas was bubbled thereinto at room temperature to the point of saturation. After keeping at room temperature for 3 days, the solution was kept at 50° C. for 6 hours. The reaction mixture was concentrated under reduced pressure, and the residue was extracted with ethyl acetate containing 1% hydrochloric acid. The organic layer was concentrated to give 2.18 g of 2-thiocarbamoyl-4′-methyl-1,1′-biphenyl. Yield, 92%; m.p., 111-115° C.; m/z, 227

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06191289B1
Source datasetuspto-grants-2001_02
ORD IDord-742ed109208f4af59c03e7b67c5ddc29
Source noteuspto-grants-2001_02