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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 914855Generated: October 25, 2026

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

https://huagongshe.com/reaction/914855

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 numberUS07265108B2
Source datasetuspto-grants-2007_09
ORD IDord-d445bdd01bee4deea3ae496410f0a6ed
Source noteuspto-grants-2007_09