HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → HCID 86755136, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | rel-(αR,βR)-β-Amino-α-hydroxybenzenepropanamide | HCID 11171329 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 86755136 | HCID 86755136 | — |
Reaction Steps
To a solution of 10.0 g of (2S, 3S) 2-hydroxy-3-amino-3-phenylpropionamide in 100 ml of methanol was slowly added 16 ml of acetyl chloride at 0° C. The reaction mixture was refluxed for 20 h then cooled to room temperature and filtered to remove the ammonium chloride salt. The filtrate was concentrated to one third of its original volume and diluted with 150 ml of ether. The precipitated salt was filtered off and washed with 100 ml of ether to give 10.6 g of methyl (2S, 3S) 2-hydroxy-3-amino-3-phenylpropionate hydrochloride as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06025516 |
| Source dataset | uspto-grants-2000_02 |
| ORD ID | ord-205eee58b90447dfbd15de4efdedb1a5 |
| Source note | uspto-grants-2000_02 |