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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 843724Generated: October 31, 2026

HCID 86584060, compound → HCID 86584059, compound

https://huagongshe.com/reaction/843724

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86584060HCID 86584060—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
ProductHCID 86584059HCID 8658405998.7%

Reaction Steps

A mixture of N-(benzyloxycarbonyl)-3(S)-phenylsulfonylmethy-β-alanine tert-butyl ester (0.44 g) and 10% Pd—C (0.1 g, 50% wet) in acetic acid (5 ml) was hydrogenated at 1 atmospheric pressure of hydrogen for 1 hour. The catalyst was filtered off and the filtrate was evaporated in vacuo. The residue was dissolved in ethyl acetate and washed with saturated aqueous NaHCO3 solution. The organic layer was dried over MgSO4 and evaporated in vacuo to give 3(S)-phenylsulfonylmethy-βalanine tert-butyl ester (0.3 g) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06380215B1
Source datasetuspto-grants-2002_04
ORD IDord-c7dd75df140f4dd49d921ef9a454e644
Source noteuspto-grants-2002_04