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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2308738Generated: November 2, 2026

Benzoyl chloride → HCID 20187548, compound

https://huagongshe.com/reaction/2308738

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 20187544HCID 20187544—
SolventDiethyl EtherHCID 3283—
ProductHCID 20187548HCID 20187548—

Reaction Steps

With efficient stirring, a solution of 25 ml of benzoyl chloride in 250 ml of diethyl ether is added dropwise at 0°-5° C. to a mixture of 250 ml of 2n NaOH solution and 27.6 g of 1-(2,4-dichlorophenyl)-2-fluoro-2-(1H-1,2,4-triazol-1-yl)ethanol (prepared in accordance with Example P1a). The reaction mixture is stirred for another 2 hours at 0°-5° C. and then further without cooling until it has reached room temperature. The separated ethereal phase is washed with four 50 ml portions of 0.2n NaOH solution and then with water until neutral, dried over sodium sulfate, filtered and concentrated by evaporation, affording as crude product 40 g of an oil which is purified by flash distillation at 0.07 mbar and 180° C. Recrystallisation from diisopropyl ether affords approx. 26 g of the product which melts at 104°-108° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04690942
Source datasetuspto-grants-1987_09
ORD IDord-20d6e54dd4154e1f863f352f57ff8c90
Source noteuspto-grants-1987_09