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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911525Generated: October 31, 2026

(S)-2-amino-3-methyl-4-phenyl-but-3-en-1-ol → (S)-2-amino-3-methyl-4-phenyl-butan-1-ol

https://huagongshe.com/reaction/1911525

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-2-amino-3-methyl-4-phenyl-but-3-en-1-olHCID 68717428—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product(S)-2-amino-3-methyl-4-phenyl-butan-1-olHCID 6871646949%

Reaction Steps

A solution of (S)-2-amino-3-methyl-4-phenyl-but-3-en-1-ol (115 mg) in EtOH (5 ml) was hydrogenated at normal pressure (balloon) overnight in the presence of 10% Pd/C (10 mg). The reaction mixture was filtered and concentrated. The crude product was purified by column chromatography (silica gel; gradient: CH2Cl2->CH2Cl2/MeOH 9:1) to give (S)-2-amino-3-methyl-4-phenyl-butan-1-ol (57 mg, 49%) as light yellow oil. MS (ISP): 180.3 ([M+H]+))

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604061B2
Source datasetuspto-grants-2013_12
ORD IDord-76fe52cc44aa4d7087dd3688eb8b7f7d
Source noteuspto-grants-2013_12