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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzoyl chloride, 3-chloro- | HCID 69252 | — |
| Reactant | Potassium thiocyanate | HCID 516872 | — |
| Reactant | 3-Chloro-5-fluoroaniline | HCID 2734838 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-Chloro-N-((3-Chloro-5-Fluorophenyl)Carbamothioyl)Benzamide | HCID 118139609 | 99.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09266839B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-716557cbeb3a4c9996cf2c703661de3d |
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| Source note | uspto-grants-2016_02 |
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