HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2280403Generated: October 30, 2026
2-Chloro-4-fluorobenzylamine → HCID 86704068, compound
https://huagongshe.com/reaction/2280403
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Chloro-4-fluorobenzylamine | HCID 139909 | — |
| Reactant | Potassium thiocyanate | HCID 516872 | — |
| Reactant | 3,4-Difluorobenzoyl chloride | HCID 2724519 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 86704068 | HCID 86704068 | 77% |
Reaction Steps
To a solution of 3,4-diflorobenzoyl chloride (45 mL, 358 mmol) in acetonitrile (1.43 L) was added solid potassium thiocyanate (KNCS) (38.2 g, 393 mmol). The suspension was stirred to 0° C. for 10 min and then the cooling bath was removed. The suspension was stirred at room temperature for an additional 20 min. A solution of 2-chloro-4-fluorobenzylamine (57.1 g, 358 mmol) in acetonitrile (150 mL) was added over 5 minutes. The resulting suspension was stirred at room temperature for 3 hours. The reaction mixture was diluted with water (1.4 L) and stirred for 1 hour. The suspension was filtered, rinsed with water (150 mL) and dried in vacuo at 60° C. to afford N-((2-chloro-4-fluorobenzyl)carbamothioyl)-3,4-difluorobenzamide as a yellow solid (98.3 g, 77% yield). 1HNMR (400 MHz, DMSO-d6) δ 11.56 (bs, 1H), 11.12 (t, 1H, J=5.7 Hz), 8.00 (m, 1H), 7.79 (m, 1H), 7.54 (m, 1H), 7.44 (m, 2H), 7.19 (m, 1H), 4.85 (d, 2H, J=5.7 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09139532B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-decc69064e8047298446919ef42e6b6a |
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| Source note | uspto-grants-2015_09 |
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