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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1004664Generated: October 29, 2026

Ethanol → HCID 10872742, compound

https://huagongshe.com/reaction/1004664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantAcetyl chlorideHCID 6367—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178520209HCID 178520209—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10872742HCID 1087274294%

Reaction Steps

At room temperature, a mixture of 1.72 g (5 mmol) of 2-(1-chloro-cyclopropyl)-1(2-chlorophenyl)-3-(5-mercapto-1,2,4-triazol-1-yl)-propan-2-ol in 20 ml of absolute tetrahydrofuran is admixed with stirring with 0.24 g (6 mmol) of sodium hydride (60% strength in paraffin oil) and stirred for 30 minutes. 0.72 ml (10 mmol) of acetyl chloride are then added and the reaction mixture is stirred at room temperature for a further 4 hours. The reaction mixture is then admixed with 1 ml of ethanol and concentrated under reduced pressure. The residue that remains is extracted repeatedly with dichloromethane. The combined organic phases are concentrated under reduced pressure. In this manner, 1.8 g (94% of theory) of 2-(1-chloro-cyclopropyl)-1-(2-chlorophenyl)-3-(5-acetylmercapto-1,2,4-triazol-1-yl)-propan-2-ol are obtained in the form of an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06051592
Source datasetuspto-grants-2000_04
ORD IDord-bbe7c4542e254229bb6f8f97212cd3b6
Source noteuspto-grants-2000_04