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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754983Generated: October 28, 2026

Sodium Hydroxide → 1-(4-Bromo-3,5-dimethylphenyl)thiourea

https://huagongshe.com/reaction/1754983

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantBenzoyl isothiocyanateHCID 68284—
Reactant4-Bromo-3,5-dimethylanilineHCID 12383117—
SolventAcetoneHCID 180—
Product1-(4-Bromo-3,5-dimethylphenyl)thioureaHCID 5088053657%

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of 4-bromo-3,5-dimethyl-phenylamine (200 mg) and benzoyl isothiocyanate (0.14 ml) in acetone (2 ml) was heated under reflux for 30 minutes. After cooling the reaction solution, a 1 N aqueous sodium hydroxide solution (2.19 ml) was added and the mixture was stirred at 50° C. for 12 hours. The mixture was extracted with dichloromethane, and the organic layer was then dried over anhydrous sodium sulfate and concentrated under reduced pressure. The resulting residue was triturated with hexane to give (4-bromo-3,5-dimethyl-phenyl)-thiourea (146 mg, 57%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169254B2
Source datasetuspto-grants-2015_10
ORD IDord-f5caee973b464469b053c447a6aa5866
Source noteuspto-grants-2015_10