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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2068684Generated: November 1, 2026

Benzoyl isothiocyanate → 1-Benzoyl-3-(5-bromo-2,4-difluoro-phenyl)-thiourea

https://huagongshe.com/reaction/2068684

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl isothiocyanateHCID 68284—
Reactant5-Bromo-2,4-difluoroanilineHCID 2783295—
SolventAcetoneHCID 180—
Product1-Benzoyl-3-(5-bromo-2,4-difluoro-phenyl)-thioureaHCID 5960309395.2%

Reaction Steps

To a solution of 5-bromo-2,4-difluoro aniline (1.0 g, 4.81 mmol) in acetone (25.0 mL) was added drop wise benzoyl isothiocyanate (0.71 mL, 5.29 mmol). The resulting reaction mixture was allowed to stir at room temperature for 30 min. After the completion of the reaction (TLC monitoring), the solvent was evaporated and the residue was washed with hexane and ether to get the title compound (1.70 g, quantitative yield) as a white solid. 1H-NMR (400 MHz, CDCl3): δ 7.02-7.06 (m, 1H), 7.56 (t, J=8.0 Hz, 2H), 7.68 (t, J=7.60 Hz, 1H), 7.91 (d, J=7.60 Hz, 2H), 8.67 (t, J=7.60 Hz, 1H), 9.15 (br s, 1H) and 12.65 (br s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299065B2
Source datasetuspto-grants-2012_10
ORD IDord-d5f114523f204b3e9e0085a9a7401caa
Source noteuspto-grants-2012_10