Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1371837Generated: October 26, 2026

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

https://huagongshe.com/reaction/1371837

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 numberUS07157488B2
Source datasetuspto-grants-2007_01
ORD IDord-70cd1c0920614208a8c92da74f201cf1
Source noteuspto-grants-2007_01