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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 724884Generated: October 31, 2026

4-Chlorobenzoyl chloride → HCID 23161670, compound

https://huagongshe.com/reaction/724884

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobenzoyl chlorideHCID 8501—
Reactant3,5-Dichlorobenzylic alcoholHCID 43236—
ReactantTBDMS etherHCID 590018—
ReactantButyllithiumHCID 178418339—
ProductHCID 23161670HCID 23161670—

Reaction Steps

Compound 26, an intermediate in the preparation of compound 1, can be prepared in several steps beginning with 3,5-dichlorobenzyl alcohol. The alcohol is protected as a t-butyldimethylsilyl ether, then treated with n-butyllithium followed by 4-chlorobenzoyl chloride to produce 4-(t-butyldimethylsilyloxymethyl-2,4',6-trichlorobenzophenone. Removal of the silyl protecting group provides compound 26.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05705514
Source datasetuspto-grants-1998_01
ORD IDord-38cadca5dfd348bc8406cdecacda3d5f
Source noteuspto-grants-1998_01