Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 712148Generated: October 29, 2026

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

https://huagongshe.com/reaction/712148

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl isothiocyanateHCID 68284—
Reactant3-(Benzyloxy)-5-bromoanilineHCID 57813626—
SolventAcetoneHCID 180—
ProductN-[(3-benzyloxy-5-bromophenyl)carbamothioyl]benzamideHCID 5781364085%

Reaction Conditions

Temperature40 °C

Reaction Steps

To a solution of 3-benzyloxy-5-bromo-aniline (480 g, 1.73 mol) in acetone (10 L) was added benzoylisothiocyanate (280 mL, 2.08 mol) at rt. After stirring the reaction mixture for 15 min, solid precipitated out and stirring was continued for 30 min at rt. After completion of reaction (by TLC), acetone was distilled off. Hexane (2 L) was added and again concentrated. To the concentrated solid was added hexane (4 L) heated to 40° C. for 30 min under stirring and the solid filtered. The solid was washed with hexane (2×2 L) to obtain the desired product (648 g, 85%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181234B2
Source datasetuspto-grants-2015_11
ORD IDord-42d1b256812e4f4bb9a9e690709e631a
Source noteuspto-grants-2015_11