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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1776995Generated: October 30, 2026

Benzoyl chloride, 3-chloro- → 3-Chloro-N-((3-Chloro-5-Fluorophenyl)Carbamothioyl)Benzamide

https://huagongshe.com/reaction/1776995

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chloride, 3-chloro-HCID 69252—
ReactantPotassium thiocyanateHCID 516872—
Reactant3-Chloro-5-fluoroanilineHCID 2734838—
SolventAcetonitrileHCID 6342—
Product3-Chloro-N-((3-Chloro-5-Fluorophenyl)Carbamothioyl)BenzamideHCID 11813960999.7%

Reaction Steps

3-Chlorobenzoyl chloride (200 g, 1.14 mol) was dissolved in acetonitrile (4.5 L) and the reaction vessel containing this mixture was cooled in an ice/water bath. Potassium thiocyanate (122 g, 1.26 mol, 1.10 equiv) was added to the reaction mixture. The cooling bath was removed from the reaction vessel after 15 minutes and the resulting slurry was stirred at room temperature for approximately 1 hour. Next, 3-chloro-5-fluoroaniline (138 mL, 1.37 mol, 1.2 equiv) was added as a solution in acetonitrile (138 mL) over 5 minutes. The reaction mixture was then stirred at room temperature overnight and subsequently quenched with water (4.30 L), and then stirred at room temperature for 1 hour. The resulting solid was collected by filtration and rinsed with acetonitrile/water (1/1 mixture by volume, 780 mL). The solid was dried at 60° C. in vacuo to provide 390 g (99% yield) of the title compound as a solid. 1H NMR (DMSO-d6) δ 12.5 (s, 1H), 11.9 (s, 1H), 8.01 (t, 1H, J=1.8), 7.89 (d, 1H, J=7.8), 7.69 (m, 3H), 7.56 (t, 1H, J=7.8), 7.34 (dt, 1H, J=8.7, 1.8). HPLC: >99% purity at 23.73 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266839B2
Source datasetuspto-grants-2016_02
ORD IDord-716557cbeb3a4c9996cf2c703661de3d
Source noteuspto-grants-2016_02