HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → HCID 86755135, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | rel-(αR,βR)-β-Amino-α-hydroxybenzenepropanamide | HCID 11171329 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86755135 | HCID 86755135 | — |
Reaction Steps
To a solution of 10.0 g of (2S, 3S) 2-hydroxy-3-amino-3-phenylpropionamide in 100 ml of ethanol was slowly added 16 ml of acetyl chloride at 0° C. The reaction mixture was refluxed for 40 h then cooled to room temperature. The reaction mixture was filtered to remove the ammonium chloride salt. The filtrate was concentrated to about one third of its original volume and diluted with 150 ml of ether. The precipitated product was filtered and washed with 100 ml of ether to give 10.9 g of ethyl (2S, 3S) 2-hydroxy-3-amino-3-phenylpropionate hydrochloride salt as a white powder, m.p. 149-151° C.; [α]D25 -25.6° (EtOH, c 1.1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06025516 |
| Source dataset | uspto-grants-2000_02 |
| ORD ID | ord-44598d87c1b346d89c82157435c6d556 |
| Source note | uspto-grants-2000_02 |