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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 496050Generated: October 26, 2026

Ammonia → 2-((Tetrahydro-2H-pyran-2-YL)oxy)cyclopropane-1-carboxamide

https://huagongshe.com/reaction/496050

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantSodium CyanideHCID 8929—
ReactantEthyl 2-(oxan-2-yloxy)cyclopropane-1-carboxylateHCID 22325102—
SolventMethanolHCID 887—
Product2-((Tetrahydro-2H-pyran-2-YL)oxy)cyclopropane-1-carboxamideHCID 22325163—

Reaction Steps

In an autoclave, a solution of 0.25 mol of the compound obtained in Step 2, 2 g of sodium cyanide, 300 ml of a 2N solution of ammonia in methanol and 80 ml of liquid ammonia is heated at 65° C. for 5 days and is then concentrated to dryness. The residue is taken up in a mixture of dichloromethane/saturated potassium carbonate solution, filtered over Celite and then treated in conventional manner. After evaporating under reduced pressure, the residue is triturated in petroleum ether, filtered, rinsed and dried, allowing the expected product to be isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06943184B2
Source datasetuspto-grants-2005_09
ORD IDord-37dccb7e6302428a9e079c22d310f0b7
Source noteuspto-grants-2005_09