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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422127Generated: November 2, 2026

o-Fluorobenzaldehyde → 2-(Diethoxymethyl)-alpha-(2-fluorophenyl)-benzenemethanol

https://huagongshe.com/reaction/1422127

Reaction equation

Participants

RoleNameHCIDCharge
Reactanto-FluorobenzaldehydeHCID 67970—
Reactant1-Bromo-2-(diethoxymethyl)benzeneHCID 3482778—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product2-(Diethoxymethyl)-alpha-(2-fluorophenyl)-benzenemethanolHCID 18357546—

Reaction Conditions

Temperature-25 °C

Reaction Steps

A solution of 345 g of 2-bromobenzaldehyde diethyl acetal in 3 l of dry tetrahydofuran was cooled to -40° C. In one portion, 913 ml of a 1.6 M solution of butyllithium in hexane were added under vigorous stirring. The resulting solution was stirred for 0.5 h at -25° C., after which a solution of 140 ml of 2-fluorobenzaldehyde in 350 ml tetrahydrofuran was added drop-wise. In a period of 4 h, the mixture was allowed to reach room temperature. The resulting mixture was pored upon ice-water and extracted several times with ethyl acetate. The organic layers were combined, washed with water, dried over magnesium sulphate and evaporated to dryness under reduced pressure to yield 404 g of 2-(diethoxymethyl)-α-(2-fluorophenyl)-benzenemethanol as an oil, M.S. (C.I.) (M/Z): 305 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06080773
Source datasetuspto-grants-2000_06
ORD IDord-1fab7de7816d4ce195a475bff72d6130
Source noteuspto-grants-2000_06