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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666780Generated: October 31, 2026

Benzaldehyde → (3-[1,3]Dioxolan-2-ylphenyl)phenylmethanol

https://huagongshe.com/reaction/1666780

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantHexaneHCID 8058—
Reactant2-(3-Bromophenyl)-1,3-dioxolaneHCID 87306—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product(3-[1,3]Dioxolan-2-ylphenyl)phenylmethanolHCID 10824966—

Reaction Steps

Combine 2-(3-bromophenyl)-1,3-dioxolane (10.0 ml, 66.0 mmol) and tetrahydrofuran (100 ml) and cool to about −78° C. Add dropwise a solution of n-butyllithium, 1.6 M solution in hexane (44.0 ml, 66.0 mmol). After 10 min, add a solution of benzaldehyde (7.6 ml, 66.0 mmol) in tetrahydrofuran (50 ml) via cannula. After 1 hour, warm to room temperature. After 18 hours, quench into water and extract with dichloromethane. Combine the organic layers and wash sequentially with distilled water and brine and then dry (Na2SO4), filter, and concentrate to give a residue. Chromatograph the residue eluting with 7:3 hexane:EtOAc to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044090B2
Source datasetuspto-grants-2011_10
ORD IDord-b97f532aec3147cd866427200825d405
Source noteuspto-grants-2011_10