Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53116Generated: October 30, 2026

Pyridine → 3-(S)-[(benzyloxycarbonyl)amino]-2-acetoxy-4-methylpentanenitrile

https://huagongshe.com/reaction/53116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetic AnhydrideHCID 7918—
Reactant3-[(Benzyloxycarbonyl)amino]-2-hydroxy-4-methylpentanenitrileHCID 15160462—
SolventEthyl AcetateHCID 8857—
Product3-(S)-[(benzyloxycarbonyl)amino]-2-acetoxy-4-methylpentanenitrileHCID 2287161794%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05618792
Source datasetuspto-grants-1997_04
ORD IDord-685e9e8f4e914f6b855025114d741b88
Source noteuspto-grants-1997_04