HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1592329Generated: October 31, 2026
Triethylamine → N-cyclopropyl-3-(4-fluorophenyl)propanamide
https://huagongshe.com/reaction/1592329
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Cyclopropylamine | HCID 69828 | — |
| Reactant | 3-(4-Fluorophenyl)propionic acid | HCID 136302 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-cyclopropyl-3-(4-fluorophenyl)propanamide | HCID 56923282 | 76.9% |
Reaction Steps
To a stirred solution of 3-(4-fluorophenyl)propionic acid (5 g, 31 mmoles) and 0.1 mL of dimethylformamide in 50 mL of anhydrous CH2Cl2 at 0° C. was added oxalyl chloride (2.84 mL, 32.6 mmoles) and the mixture was stirred for 1 hour at 0° C. and for 1 hour at room temperature. After cooling to 0° C. were added cyclopropylamine (2.6 mL, 37.2 mmoles) and triethylamine (6.5 mL, 46.5 mmoles), and the mixture was stirred for 1 hour while warming to room temperature gradually. Then water was added and the product was extracted with CH2Cl2. The extract was washed with water, dried over MgSO4 and evaporated to give a solide residue. It was recrystallized from CH2Cl2 and hexane to give 4.94 g of N-cyclopropyl-3-(4-fluorophenyl)propionamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07291744B2 |
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| Source dataset | uspto-grants-2007_11 |
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| ORD ID | ord-669fca97987a4db8868c7a78d014de78 |
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| Source note | uspto-grants-2007_11 |
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