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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2070066Generated: November 2, 2026

Benzoyl chloride → HCID 68610203, compound

https://huagongshe.com/reaction/2070066

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantHCID 67422789HCID 67422789—
SolventTetrahydrofuranHCID 8028—
SolventDiisopropylethylamineHCID 81531—
ProductHCID 68610203HCID 6861020380%

Reaction Steps

In a 25 ml round-bottomed flask, 0.5 g of 4-(2,4-bis(benzyloxy)phenyl)piperidine in 10 ml of tetrahydrofuran is dissolved in the presence of 0.26 ml of N,N-diisopropylethylamine. 0.17 ml of benzoyl chloride is added and the mixture is then stirred for 24 hours at ambient temperature. The reaction mixture is extracted with ethyl acetate and then the organic phases are combined and dried over magnesium sulphate. The residue is chromatographed on silica gel (8/2 heptane/ethyl acetate). 0.5 g of [4-(2,4-bis(benzyloxy)phenyl)piperidin-1-yl]phenylmethanone is obtained. Yield=80%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299259B2
Source datasetuspto-grants-2012_10
ORD IDord-3a2f6939469b4d189c8a2b10ba5a6115
Source noteuspto-grants-2012_10