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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 927413Generated: October 30, 2026

Triethylamine → (S)-tert-Butyl 1-cyano-2-cyclopropylethylcarbamate

https://huagongshe.com/reaction/927413

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrifluoroacetic anhydrideHCID 9845—
Reactant(S)-tert-butyl 1-amino-3-cyclopropyl-1-oxopropan-2-ylcarbamateHCID 70082562—
SolventDichloromethaneHCID 6344—
Product(S)-tert-Butyl 1-cyano-2-cyclopropylethylcarbamateHCID 7108734598.4%

Reaction Steps

To a solution of (S)-tert-butyl 1-amino-3-cyclopropyl-1-oxopropan-2-ylcarbamate (3.7 g, 16 mmol) and triethylamine (6.55 g, 65 mmol) in methylene chloride (50 mL) was added trifluoroacetic acid anhydride (6.81 g, 32 mmol) dropwise at 0° C. The resulting mixture was allowed to warm to room temperature and stirred for 4 h. The mixture was washed with water (150 mL), citric acid (150 mL, 5 M) and brine (150 mL). The organic phase was dried over anhydrous sodium sulfate and concentrated to give product (3.31 g, 97%) as a yellow solid; MS (EI): m/e 233.1 [M+Na]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290451B2
Source datasetuspto-grants-2016_03
ORD IDord-27a5d5ee619149a0933fd532ea804d8b
Source noteuspto-grants-2016_03