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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010684Generated: October 31, 2026

Benzoyl isothiocyanate → N-[(3-benzyloxy-5-bromophenyl)carbamothioyl]benzamide

https://huagongshe.com/reaction/1010684

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl isothiocyanateHCID 68284—
Reactant3-(Benzyloxy)-5-bromoanilineHCID 57813626—
SolventAcetoneHCID 180—
ProductN-[(3-benzyloxy-5-bromophenyl)carbamothioyl]benzamideHCID 5781364089%

Reaction Steps

To a solution of 3-benzyloxy-5-bromo-phenylamine (23.50 g, 84.40 mmol) in acetone (550.0 mL) was added benzoyl isothiocyanate (18.50 mL, 93.13 mmol) and the reaction mixture was stirred at room temperature for 30 min. After the completion of the reaction (TLC monitoring), the solvent was evaporated and the residue thus obtained was washed with hexane to get the desired product (33.0 g, 89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977340B2
Source datasetuspto-grants-2011_07
ORD IDord-36c4fb42e2de4ff893242813afa30586
Source noteuspto-grants-2011_07