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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2374845Generated: October 30, 2026

Cyclohexanol → HCID 13240890, compound

https://huagongshe.com/reaction/2374845

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanolHCID 7966—
ReactantEthyl isocyanatoacetateHCID 76283—
SolventDichloromethaneHCID 6344—
ProductHCID 13240890HCID 13240890—

Reaction Steps

620 mg (4.80 mmol) of ethyl isocyanatoacetate was dissolved in 5 ml of dichloromethane. 10 ml of a solution of 0.56 ml (5.28 mmol) of cyclohexanol in 10 ml of dichloromethane was added to the obtained solution under cooling with ice, and they were stirred at room temperature for 15 minutes. The reaction mixture was concentrated under reduced pressure. 5.8 ml of 1 N aqueous lithium hydroxide solution was added to the concentrate, and the obtained mixture was stirred in a solvent mixture of methanol:water=2:1 at room temperature for 2 hours. The reaction mixture was concentrated under reduced pressure. Water was added to the concentrate and the resultant aqueous layer was washed with ethyl acetate. 0.1 N aqueous hydrochloric acid solution was added to the aqueous layer to control pH at 2 to 3. After extracting with ethyl acetate, the organic layer was dried over anhydrous magnesium sulfate and then concentrated under reduced pressure to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07462630B2
Source datasetuspto-grants-2008_12
ORD IDord-60f0c9302d574741a82a19ab8461c926
Source noteuspto-grants-2008_12