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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1187769Generated: November 1, 2026

HCID 67156334, compound → HCID 67151537, compound

https://huagongshe.com/reaction/1187769

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67156334HCID 67156334—
CatalystPlatinumHCID 23939—
SolventMethanolHCID 887—
ProductHCID 67151537HCID 6715153778%

Reaction Steps

To a solution of [(E)-(S)-3-(4-bromo-phenyl)-1-hydroxymethyl-allyl]-carbamic acid tert-butyl ester (14.7 g) in methanol (150 ml) was added 10% Pt/C (1.68 g) and the resulting mixture was stirred under a H2 balloon at room temperature for 3 hours (whereby the reaction progress was checked continuously by 1H NMR). The reaction mixture was filtered through celite and the filtrate was concentrated in vacuo to afford [(S)-3-(4-bromo-phenyl)-1-hydroxymethyl-propyl]-carbamic acid tert-butyl ester as a yellow solid (11.5 g, 78%). MS (ISP): 346.0 ([{81Br}M+H]+), 344.0 ([{79Br}M+H]+), 289.9 ([{81Br}M+H—C4H8]+), 288.0 ([{79Br}M+H—C4H8]+), 246.1 ([{81Br}M+H—C4H8—CO2]+), 244.1 ([{79Br}M+H—C4H8—CO2]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673950B2
Source datasetuspto-grants-2014_03
ORD IDord-142f11039f6e4b039f4d800691e50ee9
Source noteuspto-grants-2014_03