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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1994125Generated: November 2, 2026

Acetic Acid → tert-butyl N-[(2S)-1-{[(tert-butoxy)carbonyl]amino}-3-hydroxypropan-2-yl]carbamate

https://huagongshe.com/reaction/1994125

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantLithium ChlorideHCID 433294—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86606495HCID 86606495—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
Producttert-butyl N-[(2S)-1-{[(tert-butoxy)carbonyl]amino}-3-hydroxypropan-2-yl]carbamateHCID 8660649672.3%

Reaction Steps

To a solution of methyl (2S)-2,3-bis[(tert-butoxycarbonyl)amino]-propanoate (3.57 g, 11.2 mmol) in THF (60 mL) at 0° C. was added lithium chloride (523 mg, 12.3 mmol) and then sodium borohydride (467 mg, 12.3 mmol) portionwise. Ethanol (30 mL) was added slowly. The reaction mixture was allowed to warm to rt and stirred for 18 h. Acetic acid (0.707 mL, 12.3 mmol) was added and the solvents were evaporated. The residue was purified by chromatography (SiO2, EtOAc/hexane) to yield the title compound as a white solid (2.35 g, 72.2%). LCMS: (FA) ES+ 291.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652041B2
Source datasetuspto-grants-2010_01
ORD IDord-1c06efc9f3db4ec1a0d2f702ec34232f
Source noteuspto-grants-2010_01