HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzylamine → n-benzyl-3-bromopropanamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Propanoyl chloride, 3-bromo- | HCID 84944 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | n-benzyl-3-bromopropanamide | HCID 236377 | — |
Reaction Steps
A solution of benzylamine (6.49 ml) and triethylamine (8.26 ml) in ethyl acetate (60 ml) was added dropwise to a solution of 3-bromopropionyl chloride (6 ml) in ethyl acetate (10 ml) at 0° C. The reaction mixture was stirred to room temperature for 1 hr. The organic phase was washed with water (2×150 ml), saturated brine (150 ml) and dried over magnesium sulphate. Removal of the solvent produced the amide as a crystalline solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04524073 |
| Source dataset | uspto-grants-1985_06 |
| ORD ID | ord-81f45aacaa964f2ca0c63aec49653c04 |
| Source note | uspto-grants-1985_06 |