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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1510341Generated: October 26, 2026

Sodium Cyanide → tert-Butyl 1-(1-amino-1-cyanoethyl)-1-cyclopropanecarboxylate

https://huagongshe.com/reaction/1510341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CyanideHCID 8929—
ReactantAmmonium ChlorideHCID 25517—
Reactanttert-Butyl 1-acetylcyclopropanecarboxylateHCID 57434365—
SolventAmmoniaHCID 222—
SolventMethanolHCID 887—
Producttert-Butyl 1-(1-amino-1-cyanoethyl)-1-cyclopropanecarboxylateHCID 57434366—

Reaction Steps

tert-Butyl 1-acetyl-1-cyclopropanecarboxylate (9.21 g, 50.0 mmol) was dissolved in a 7N solution of ammonia in methanol (300 mL), and to this solution in an ice bath were added concentrated ammonia solution (90 mL), ammonium chloride (53.5 g, 1.00 mol), and sodium cyanide (4.90 g, 100.0 mmol). The mixture was stirred at room temperature for 18 hours, and the solvent was concentrated under reduced pressure. To the concentrate was added water (100 mL), and the solution was extracted with dichloromethane (300 mL+2×100 mL). The organic layers were combined, and dried by adding anhydrous sodium sulfate. After removing the dessicating agent by filtration, the solvent was removed by distillation under reduced pressure to obtain 10.15 g (48.3 mmol, 97%) of the crude target compound as a pale brown oil. The thus obtained crude product was used in the subsequent reaction with no further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08211910B2
Source datasetuspto-grants-2012_07
ORD IDord-b6965ac5492d466cb99154783d07e2b9
Source noteuspto-grants-2012_07