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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2365912Generated: November 2, 2026

Benzoyl chloride → HCID 68610203, compound

https://huagongshe.com/reaction/2365912

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 numberUS08697726B2
Source datasetuspto-grants-2014_04
ORD IDord-6f2a789bfa2743028d4712555b4bf10f
Source noteuspto-grants-2014_04