HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 3-(S)-[(benzyloxycarbonyl)amino]-2-acetoxy-4-methylpentanenitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 3-[(Benzyloxycarbonyl)amino]-2-hydroxy-4-methylpentanenitrile | HCID 15160462 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-(S)-[(benzyloxycarbonyl)amino]-2-acetoxy-4-methylpentanenitrile | HCID 22871617 | 94% |
Reaction Steps
To a solution containing 3-[(benzyloxycarbonyl)amino]-2-hydroxy-4-methylpentanenitrile (32.0 g, 0.12 mol) and pyridine (59 mL) was added acetic anhydride (73.6 g, 68 mL, 0.72 mol) dropwise at RT. After 3 h the reaction was diluted with ethyl acetate and washed with water. The organic layer was separated, dried (anhydrous magnesium sulfate) and evaporated. The residue was purified by column chromatography (silica get, 1:1 hexane:ethyl acetate) to give 33.08 g (94.0%) of 3-(S)-[(benzyloxycarbonyl)amino]-2-acetoxy-4-methylpentanenitrile as a viscous yellow oil; TLC Rf =0.70 (silica gel, 1:1 hexane:ethyl acetate).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05618792 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-685e9e8f4e914f6b855025114d741b88 |
| Source note | uspto-grants-1997_04 |