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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 329198Generated: October 31, 2026

Chloroacetonitrile → HCID 21438990, compound

https://huagongshe.com/reaction/329198

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetonitrileHCID 7856—
ReactantPotassium ethoxideHCID 23670592—
ReactantHCID 53693398HCID 53693398—
SolventMethanolHCID 887—
ProductHCID 21438990HCID 2143899040.6%

Reaction Steps

A suspension of 38.3 g of cyclohexyl N-carbethoxy-thiocarbamate and 11.56 g of potassium ethylate in 400 ml of methanol was stirred for 2 hours and 12.45 g of chloroacetonitrile were added thereto. The mixture was stirred for 48 hours at room temperature and was then concentrated to dryness. The residue was added to water and the aqueous phase was acidified with hydrochloric acid. The aqueous phase was extracted with ether and the ether phase was dried and concentrated to dryness to obtain 15 g of 2-cyclohexyloxy-4-hydroxy-5-cyanothiazole in the form of white crystals melting at 138° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04020076
Source datasetuspto-grants-1977_04
ORD IDord-41e5b5170ad14c9e836b0918f2446005
Source noteuspto-grants-1977_04