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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1508278Generated: November 2, 2026

Water → tert-butyl N-((1S)-1-cyanoethyl)carbamate

https://huagongshe.com/reaction/1508278

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCyanuric chlorideHCID 7954—
ReactantBoc-Ala-NH2HCID 7015295—
SolventDimethylformamideHCID 6228—
Producttert-butyl N-((1S)-1-cyanoethyl)carbamateHCID 63838363%

Reaction Steps

To a stirred solution of tert-butyl [(1S)-2-amino-1-methyl-2-oxoethyl]carbamate (Step 1, 0.7 g, 0.004 mol) in N,N-dimethylformamide (5 mL) was added 343 mg of cyanuric chloride (0.00186 mol) at once. The reaction mixture was stirred for 4 h. Water was added and the mixture was extracted with ethyl acetate. The combined organic layers were washed with brine, dried over MgSO4, filtered, and concentrated under reduced pressure. The residue was purified by flash chromatography on a silica gel column with EtOAc in hexane (30-50%) to yield the desired product (400 mg, 63%). 1H-NMR (300 MHz, DMSO-d6): 7.74 (d, J=7.0 Hz, 1H), 4.48 (m, 1H), 1.40 (s, 9H), 1.35 (d, J=7.0 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221824B2
Source datasetuspto-grants-2015_12
ORD IDord-dd77eb606b1140678a9674ffd9f7b3b1
Source noteuspto-grants-2015_12