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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1689459Generated: October 30, 2026

Dimethylformamide → 5-(2-(tert-Butyldimethylsilyloxy)ethyl)-2-fluorobenzaldehyde

https://huagongshe.com/reaction/1689459

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPentamethyldiethylenetriamineHCID 18196—
Reactanttert-Butyl(4-fluorophenethoxy)dimethylsilaneHCID 57989254—
ReactantCID 53628100HCID 178418400—
SolventTetrahydrofuranHCID 8028—
Product5-(2-(tert-Butyldimethylsilyloxy)ethyl)-2-fluorobenzaldehydeHCID 57989066—

Reaction Conditions

Temperature-78 °C

Reaction Steps

sec-Butyllithium (1.4M in cyclohexane, 2.78 ml) was added to dry tetrahydrofuran (10 mL) under nitrogen and the solution cooled to −78° C. N1-(2-(dimethylamino)ethyl)-N1,N2,N2-trimethylethane-1,2-diamine (0.674 g) was added slowly dropwise. A solution of tert-butyl(4-fluorophenethoxy)dimethylsilane (example 100, step a) (0.99 g) in dry tetrahydrofuran (3 mL) was then added dropwise over 5 minutes. Reaction mixture stirred for 2 hours at −78° C. DMF (2.1 ml) was added dropwise over 5 minutes and the mixture stirred at −78° C. for 1 hour followed by room temperature for 45 minutes. The reaction mixture was quenched by addition of water. Ethyl acetate (200 mL) was added and the organic washed three times with water, followed by twice with 2M HCl and then twice with water. The organic solution was washed with brine, dried over sodium sulphate, filtered and evaporated under reduced pressure. The crude product was purified by flash silica chromatography using 2% ethyl acetate in isohexane as solvent. Pure fractions were evaporated to dryness to afford the subtitled compound. Yield 0.5 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08148373B2
Source datasetuspto-grants-2012_04
ORD IDord-33e629a3f7184008bdbf4624c0607800
Source noteuspto-grants-2012_04