HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1914664Generated: October 31, 2026
2-Chloro-5-(trifluoromethyl)benzoyl chloride → 2-Chloro-N-(2-methyl-4-phenylaminomethyl-cyclohexyl)-5-trifluoromethyl-benzamide
https://huagongshe.com/reaction/1914664
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Chloro-5-(trifluoromethyl)benzoyl chloride | HCID 2778106 | — |
| Reactant | (4-Amino-3-methyl-cyclohexylmethyl)-phenyl-amine | HCID 67185375 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Chloro-N-(2-methyl-4-phenylaminomethyl-cyclohexyl)-5-trifluoromethyl-benzamide | HCID 44816139 | — |
Reaction Steps
(4-Amino-3-methyl-cyclohexylmethyl)-phenyl-amine (113 mg, 0.52 mmol) in dry THF (5 mL) and TEA (105 mg, 1.04 mmol) is treated with 2-chloro-5-(trifluoromethyl)benzoyl chloride (139 mg, 0.57 mmol). After stirring at RT for 2 hours, the solvent is removed in vacuo and the residue is partitioned between water and DCM. The mixture is passed through a phase separator and the organic portion is concentrated in vacuo. Purification of the crude residue by chromatography on silica eluting with iso-hexane:EtOAc (9:1 increasing to 2:1) affords the title compound. 1H NMR (400 MHz, DMSO-d6) δ 8.47 (1H, d), 7.82 (1H, d), 7.73 (2H, m), 7.07 (2H, t), 6.56 (2H, d), 6.49 (1H, t), 5.55 (1H, m), 3.93 (1H, m), 2.86 (2H, m), 2.23 (1H, m), 1.88 (1H, m), 1.78 (1H, m), 1.70 (1H, m), 1.59 (2H, m), 1.31 (1H, m), 1.11 (1H, m), 0.92 (3H, d).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08614213B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-23707da03eb44902bb504bf445218e87 |
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| Source note | uspto-grants-2013_12 |
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