HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 445295Generated: October 30, 2026
4-(Trifluoromethyl)benzoyl chloride → HCID 9051890, compound
https://huagongshe.com/reaction/445295
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-(Trifluoromethyl)benzoyl chloride | HCID 67607 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-(3-Fluorophenyl)ethanamine | HCID 533928 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 9051890 | HCID 9051890 | — |
Reaction Steps
A 250-mL, round-bottomed flask containing a solution of 2-(3-fluorophenyl)ethanamine (1.3 mL, 9.6 mmol) and diisopropylethylamine (1.7 mL, 9.6 mmol) in dichloromethane (32 mL) was cooled to 0° C. and treated dropwise with 4-(trifluoromethyl)benzoyl chloride (2.0 mL, 9.6 mmol) over 5 min. The ice-bath was removed after 2 h and the reaction mixture was stirred overnight. The precipitate formed was collected by filtration. The filtrate was diluted with dichloromethane (100 mL) and transferred to a separatory funnel and extracted with water (35 mL). The dichloromethane layer was separated and formation of precipitate was observed which was collected by filtration. The filtrate was concentrated to yield more solid and the combined solids were dried under vacuum to yield N-(3-fluorophenethyl)-4-(trifluoromethyl)benzamide as a white solid. MS (ESI pos. ion) m/z: 312 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08476297B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-610b75128ad947a3b3d632a90f6cb371 |
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| Source note | uspto-grants-2013_07 |
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