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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 29189Generated: October 25, 2026

Isopropanol → tert-Butyl-N-((1S,2R)-1-benzyl-3-(tert-butyloxy)amino-2-hydroxypropyl)carbamate

https://huagongshe.com/reaction/29189

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
ReactantDiisopropylethylamineHCID 81531—
ReactantO-tert-butylhydroxylamine hydrochlorideHCID 2777906—
Reactant(1S)-1-[(2S)oxiranyl]-2-phenylethylcarbamateHCID 20638362—
Producttert-Butyl-N-((1S,2R)-1-benzyl-3-(tert-butyloxy)amino-2-hydroxypropyl)carbamateHCID 59090702—

Reaction Steps

tert-Butyl-N-((1S)-1-[(2S)oxiranyl]-2-phenylethylcarbamate (0.155 g, 0.59 mmol) and O-(tert-butyl)hydroxylamine hydrochloride (0.089 g, 0.71 mmol) were heated with diisopropylethylamine (0.154 ml, 0.88 mmol) in isopropanol (2 ml) in a sealed tube at 60° C. for 5 days. The reaction mixture was concentrated in vacuo, taken up in EtOAc, washed with sat. aq. NaHCO3, and brine. The organic phase was dried over MgSO4, filtered and solvent removed in vacuo. Purication by column chromatography (1% MeOH in CH2Cl2) gave 100 mg of a white solid which was used directly in the next reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07419967B2
Source datasetuspto-grants-2008_09
ORD IDord-52b8f8f029684768afcaa2b5b52f915e
Source noteuspto-grants-2008_09