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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 890067Generated: October 27, 2026

Water → (1-Benzylpiperidin-4-yl)-(1,3-dihydroisobenzofuran-1-yl)methanol

https://huagongshe.com/reaction/890067

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
Reactant1,3-DihydroisobenzofuranHCID 10327—
Reactant1-Benzylpiperidine-4-carbaldehydeHCID 89584—
SolventTetrahydrofuranHCID 8028—
SolventButyllithiumHCID 178418339—
Product(1-Benzylpiperidin-4-yl)-(1,3-dihydroisobenzofuran-1-yl)methanolHCID 2224846537.5%

Reaction Conditions

Temperature-70 °C

Reaction Steps

After dissolving 591 mg of 1,3-dihydroisobenzofuran in 10 ml of tetrahydrofuran, 3.9 ml of n-butyllithium (1.5 M, n-hexane solution) was added thereto at −70° C. under a nitrogen atmosphere, the mixture was stirred for 1 hour, and then a solution of 1 g of 1-benzylpiperidine-4-carboxaldehyde in tetrahydrofuran (5 ml) was added dropwise and the mixture was stirred for 1 hour. Water was added to the reaction solution, extraction was performed with ethyl acetate, the extract was dried over anhydrous magnesium sulfate, and then the solvent was distilled off under reduced pressure. Purification was performed by silica gel column chromatography (solvent: n-hexane/ethyl acetate) to obtain 597 mg of (1-benzylpiperidin-4-yl)-(1,3-dihydroisobenzofuran-1-yl)methanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06995144B2
Source datasetuspto-grants-2006_02
ORD IDord-b9a9d7ccb3224e999e73bdc462941551
Source noteuspto-grants-2006_02