HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1788042Generated: October 30, 2026
Trichloroacetyl chloride → 2,2,2-trichloro-N-[2-(3-chlorobenzoyl)-4-(4-fluorobenzoyl)phenyl]-acetamide
https://huagongshe.com/reaction/1788042
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trichloroacetyl chloride | HCID 6420 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | [2-Amino-5-(4-fluorobenzoyl)phenyl](3-chlorophenyl)-methanone | HCID 17976107 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,2,2-trichloro-N-[2-(3-chlorobenzoyl)-4-(4-fluorobenzoyl)phenyl]-acetamide | HCID 68688854 | 95.5% |
Reaction Steps
Trichloro-acetylchloride (0.0848 mol) was added dropwise at 5° C. to a mixture of intermediate 3 (0.0707 mol) in DCM (250 ml) under N2 flow. The mixture was stirred at 5° C. for 30 minutes. Triethylamine (0.0848 mol) was added dropwise at 5° C. The mixture was stirred at 5° C. for 1 hour, then at room temperature for 2 hours and poured out into ice water. DCM was added. The mixture was extracted with DCM. The organic layer was separated, dried (MgSO4), filtered and the solvent was evaporated. The residue was crystallized from diethyl ether/DIPE. The precipitate was filtered off and dried, yielding 33.7 g (95%) of 2,2,2-trichloro-N-[2-(3-chlorobenzoyl)-4-(4-fluorobenzoyl)phenyl]-acetamide (intermediate 4).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07511138B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-03857d6b9804438ab847be67069e97ee |
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| Source note | uspto-grants-2009_03 |
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