HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 445299Generated: October 30, 2026
p-Fluorophenethylamine → HCID 7935360, compound
https://huagongshe.com/reaction/445299
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Fluorophenethylamine | HCID 4653 | — |
| Reactant | 4-(Trifluoromethyl)benzoyl chloride | HCID 67607 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 7935360 | HCID 7935360 | — |
Reaction Steps
A 250-mL, round-bottomed flask containing a solution of 4-fluorophenethylamine (4.8 mL, 37 mmol) and diisopropylethylamine (6.4 mL, 37 mmol) in dichloromethane (40 mL) was cooled to 0° C. and treated dropwise with 4-(trifluoromethyl)benzoyl chloride (5.5 mL, 37 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, extracted with water (35 mL), brine (25 mL), and 1N HCl (25 mL). The dichloromethane layer was separated and formation of more precipitate was observed which was collected by filtration. The solids collected were combined and dried under vacuum to yield N-(4-fluorophenethyl)-4-(trifluoromethyl)benzamide as an off-white solid. MS (ESI pos. ion) m/z: 312 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08476297B2 |
|---|
| Source dataset | uspto-grants-2013_07 |
|---|
| ORD ID | ord-130f064c968347e7b6b87e75f5c8b373 |
|---|
| Source note | uspto-grants-2013_07 |
|---|