HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1765804Generated: October 30, 2026
Oxalyl chloride → 3-bromo-N-cyclopropyl-4-methylbenzamide
https://huagongshe.com/reaction/1765804
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Cyclopropylamine | HCID 69828 | — |
| Reactant | 3-Bromo-4-methylbenzoic acid | HCID 82130 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-bromo-N-cyclopropyl-4-methylbenzamide | HCID 21107152 | — |
Reaction Steps
A stirred, cooled (ice bath) solution of 3-bromo-4-methyl-benzoic acid (Aldrich, 5 g, 23.25 mmol) in benzene (50 mL), dichloromethane (10 mL) and N,N-dimethylformamide (0.5 mL) was treated with oxalyl chloride (4 mL, 46.5 mmol). The reaction mixture was allowed to warm to ambient temperature over 3 h. The volatiles were then distilled off in vacuo, the residue was diluted with anhydrous dichloromethane (50 mL) under argon, cooled (ice bath) and treated with 4-(dimethylamino)pyridine (5.67 g, 46.5 mmol) followed by cyclopropyl amine (1.93 mL, 27.9 mmol). After 3 h, the reaction mixture was diluted with dichloromethane and washed with water. The organic phase was dried-over anhydrous sodium sulfate, filtered and evaporated in vacuo to afford the title product that was used as such for the next step (6.0 g,˜100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07226951B2 |
|---|
| Source dataset | uspto-grants-2007_06 |
|---|
| ORD ID | ord-23927d08b2ed42629b68dd3b09d2c3eb |
|---|
| Source note | uspto-grants-2007_06 |
|---|