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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569757Generated: October 30, 2026

t-Butyl alpha-[3(S*)-azido-2-oxo-6(R*)-phenylperhydroazepin-1-yl]acetate → t-Butyl alpha-[3(S*)-amino-2-oxo-6(R*)-phenylperhydroazepin-1-yl]acetate

https://huagongshe.com/reaction/569757

Reaction equation

Participants

RoleNameHCIDCharge
Reactantt-Butyl alpha-[3(S*)-azido-2-oxo-6(R*)-phenylperhydroazepin-1-yl]acetateHCID 14003443—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Productt-Butyl alpha-[3(S*)-amino-2-oxo-6(R*)-phenylperhydroazepin-1-yl]acetateHCID 14003450—

Reaction Steps

0.3 g of 5% w/w palladium-on-carbon was added to 30 ml of ethanol containing 1.4 g of t-butyl α-[3(S*)-azido-2-oxo-6(R*)-phenylperhydroazepin-1-yl]acetate (Isomer A) [prepared as described in Example 1(h)], and under one atmosphere pressure of hydrogen the reaction mixture was shaken for 4 hours at 40° C. The catalyst was filtered off and the solvent was evaporated under reduced pressure, to give 1.56 g of the title compound as a gummy substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04734410
Source datasetuspto-grants-1988_03
ORD IDord-937c9b542ff5470289cf2296ca2abbce
Source noteuspto-grants-1988_03