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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57404Generated: October 28, 2026

Hydrazine → tert-butyl N-((1S)-1-(hydrazinecarbonyl)ethyl)carbamate

https://huagongshe.com/reaction/57404

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazineHCID 9321—
ReactantBoc-L-alanine methyl esterHCID 10856577—
SolventTetrahydrofuranHCID 8028—
Producttert-butyl N-((1S)-1-(hydrazinecarbonyl)ethyl)carbamateHCID 10241974—

Reaction Steps

A solution of (S)-methyl 2-((tert-butoxycarbonyl)amino)propanoate (1.00 g, 4.92 mmol) and hydrazine (0.23 mL, 1.5 equiv) in THF (8 mL) was heated in a sealed tube at 72° C. for 15 hours. Additional hydrazine (0.23 mL, 1.5 equiv) was added and heating was continued for another 21 hours. The reaction was then cooled to room temperature and concentrated in vacuo to give crude (S)-tert-butyl(1-hydrazinyl-1-oxopropan-2-yl)carbamate (1 g, white solid), which was used without purification. 1H NMR (400 MHz, CDCl3) δ 4.20 (m, 1H), 1.44 (s, 9H), 1.36 (d, J=7.1 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434719B2
Source datasetuspto-grants-2016_09
ORD IDord-af3f2e06c332425aab8953dc44bfeb70
Source noteuspto-grants-2016_09