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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1291195Generated: November 2, 2026

Water → 4-Piperidinemethanol, 1-benzoyl-

https://huagongshe.com/reaction/1291195

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTrimethyl borateHCID 8470—
ReactantEthyl 1-benzoylpiperidine-4-carboxylateHCID 735824—
ReactantTrilithium borateHCID 13743157—
SolventTetrahydrofuranHCID 8028—
Product4-Piperidinemethanol, 1-benzoyl-HCID 1026287090%

Reaction Steps

10.4 g (0.04 mol) of ethyl 1-benzoyl-4-piperidine-carboxylate were dissolved in 90 ml of THF and treated with a solution of 0.871 g (0.04 mol) of lithium borate in 20 ml of THF. 0.45 ml (0.004 mol) of trimethyl borate was added and the mixture was stirred at room temperature for 60 hrs. The reaction mixture was treated with water and stirred for 1.5 hrs. The mixture was extracted with ethyl acetate and the organic phase was washed with water and saturated sodium chloride solution and dried over sodium sulfate. The residue was chromatographed on silica gel with ethyl acetate/hexane (1:1). 7.8 g (90%) of 1-benzoyl-4-hydroxymethyl-piperidine were obtained as white crystals; m.p. 84°-87°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05753679
Source datasetuspto-grants-1998_05
ORD IDord-7f6c9900f2484e1da42ec8aeb541153a
Source noteuspto-grants-1998_05