Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1689289Generated: October 25, 2026

Dimethylformamide → 3-(2-(tert-Butyldimethylsilyloxy)-1-fluoroethyl)benzaldehyde

https://huagongshe.com/reaction/1689289

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant(2-(3-Bromophenyl)-2-fluoroethoxy)(tert-butyl)dimethylsilaneHCID 57989324—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product3-(2-(tert-Butyldimethylsilyloxy)-1-fluoroethyl)benzaldehydeHCID 57989201—

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of (2-(3-bromophenyl)-2-fluoroethoxy)(tert-butyl)dimethylsilane (example 39, step c) (1.8 g) in THF (36 mL) was cooled to −78° C. under an atmosphere of nitrogen and treated with butyllithium (1.8M in hexanes, 3.3 mL), added dropwise over 5 minutes. The solution was stirred at −78° C. for 30 minutes, treated with N,N-dimethylformamide (0.63 mL), stirred at −78° C. for a further 30 minutes, then removed from the cooling bath and allowed to warm to room temperature over 140 minutes. The solution was quenched by the addition of 10% aqueous ammonium chloride, and the resulting mixture was extracted twice with diethyl ether. The combined organic phases were washed with brine, dried over anhydrous magnesium sulphate and purified by flash chromatography on silica eluted with 50% dichloromethane in isohexane to afford the subtitled compound as a colourless oil. Yield 1.26 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08148373B2
Source datasetuspto-grants-2012_04
ORD IDord-70ccd8263d074370b4a469ecc1e30aac
Source noteuspto-grants-2012_04