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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 722823Generated: October 31, 2026

(2S,3S)-2-(N-Benzyloxycarbonylamino)-3-octadecanol → (2S,3S)-2-Amino-3-octadecanol

https://huagongshe.com/reaction/722823

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2S,3S)-2-(N-Benzyloxycarbonylamino)-3-octadecanolHCID 58743388—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product(2S,3S)-2-Amino-3-octadecanolHCID 5701770089%

Reaction Steps

To a solution of N-benzyloxycarbonylamine 90 (330 mg, 0.79 mmol) in MeOH (40 mL) at room temperature, Pd—C (10% wt, 100 mg, 0.09 mmol) was added. The mixture was purged with a stream of dry Ar, and then H2. The reaction was stirred overnight under a H2 atmosphere (1 atm). The catalyst was filtered off through a 0.45 μm teflon filter in polypropylene housing, washing the filter with MeOH (50 mL) and the solvent was evaporated in vacuo. The crude was purified by column chromatography on silica (90:10 CH2Cl2/MeOH to 100% MeOH) to obtain aminoalcohol 91 as a white solid (200 mg, 89% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07138547B2
Source datasetuspto-grants-2006_11
ORD IDord-83630ad523ed493bb455ccf9435fdefb
Source noteuspto-grants-2006_11