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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1811738Generated: November 2, 2026

(R)-tert-Butyl (oxiran-2-ylmethyl)carbamate → (3-Amino-2-hydroxy-propyl)-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/1811738

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-tert-Butyl (oxiran-2-ylmethyl)carbamateHCID 10464779—
ReactantAzane;hydrateHCID 12896473—
SolventEthanolHCID 702—
Product(3-Amino-2-hydroxy-propyl)-carbamic acid tert-butyl esterHCID 86639750—

Reaction Steps

(R)-1-Oxiranylmethylcarbamic acid tert-butyl ester (2.26 g, 13.05 mmol) obtained in Step 2 above was dissolved in ethanol (15 ml), and then 28% ammonia water (6 ml) was added thereto at room temperature. After the solution was stirred at room temperature for 1.5 hour, the solvent was distilled off under reduced pressure. After the resulting residue was dissolved in methanol, the solvent was distilled off under reduced pressure to give a crude product of ((S)-3-amino-2-hydroxypropyl)carbamic acid tert-butyl ester (2.38 g) as a yellow oily material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362236B2
Source datasetuspto-grants-2013_01
ORD IDord-57297dafbb8d47b2b63ad80ded3b37ee
Source noteuspto-grants-2013_01