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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1636887Generated: November 2, 2026

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

https://huagongshe.com/reaction/1636887

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 gel, 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 numberUS06037325
Source datasetuspto-grants-2000_03
ORD IDord-bc2455e2d1594d97a0a1426800014a40
Source noteuspto-grants-2000_03