HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl bromide → O-acetyl-N-benzyloxycarbonyl-L-threonine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl bromide | HCID 10482 | — |
| Reactant | N-((Benzyloxy)carbonyl)-L-threonine | HCID 88217 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | O-acetyl-N-benzyloxycarbonyl-L-threonine | HCID 18640002 | — |
Reaction Steps
To a solution of N-benzyloxycarbonyl-L-threonine (5 g) in acetic acid (50 ml) was added acetyl bromide (1.75 ml) at room temperature. After stirring for an hour at room temperature, the reaction mixture was concentrated and the residue was diluted with ethyl acetate and washed successively with water (2 times) and brine. After drying over sodium sulfate, the ethyl acetate extract was filtered and concentrated to give O-acetyl-N-benzyloxycarbonyl-L-threonine (3.64 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04939241 |
| Source dataset | uspto-grants-1990_07 |
| ORD ID | ord-6db671a105ea4ab58a2b9cebaa021144 |
| Source note | uspto-grants-1990_07 |