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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1480124Generated: October 26, 2026

Benzyl chloroformate → (1-Cyano-2-cyclopropyl-1-methyl-ethyl)-carbamic acid benzyl ester

https://huagongshe.com/reaction/1480124

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Amino-3-cyclopropyl-2-methyl-propionitrileHCID 84716049—
SolventTetrahydrofuranHCID 8028—
Product(1-Cyano-2-cyclopropyl-1-methyl-ethyl)-carbamic acid benzyl esterHCID 9020403460%

Reaction Conditions

Temperature45 °C

Reaction Steps

To a solution of 2-Amino-3-cyclopropyl-2-methyl-propionitrile (Example 66a, 5.01 g, 30.9 mmol) in dry THF (119 mL) was added DIEA (12.1 mL, 67.9 mmol) and benzyl carbonochloridate (CAN 501-53-1, 5.57 mL, 37.1 mmol). The reaction was stirred at 45° C. for 18 hours. The reaction mixture was concentrated under reduced pressure. The residue was dissolved in ethylacetate and extracted with an 1.0M aqueous solution of sodium bicarbonate. The organic layer was dried over sodium sulfate and evaporated down to dryness. The crude material was purified by flash chromatography eluting with a gradient of heptane/ethylacetate to yield the title compound (6.2, 60%) as a colorless oil. MS (ESI, m/z): 259.5 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409866B2
Source datasetuspto-grants-2016_08
ORD IDord-05123ffb9a4543f9a9175e88a87b33c5
Source noteuspto-grants-2016_08