Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2267341Generated: October 30, 2026

Ammonium Chloride → (3-(2-(tert-Butyldimethylsilyloxy)ethyl)thiophen-2-yl)(4-fluorophenyl)methanol

https://huagongshe.com/reaction/2267341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant4-FluorobenzaldehydeHCID 68023—
Reactant(2-(2-Bromothiophen-3-yl)ethoxy)(tert-butyl)dimethylsilaneHCID 60204457—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product(3-(2-(tert-Butyldimethylsilyloxy)ethyl)thiophen-2-yl)(4-fluorophenyl)methanolHCID 6020445859%

Reaction Conditions

Temperature-78 °C

Reaction Steps

n-Butyllithium in hexanes (12.7 mL, 1.6 M, 20.3 mmol) was added dropwise to a solution of (2-(2-bromothiophen-3-yl)ethoxy)(tert-butyl)dimethylsilane (5.9 g, 18.4 mmol) in anhydrous THF (15 mL) at −78° C. The resulting mixture was stirred at −78° C. for 30 min and 4-fluorobenzaldehyde (2.5 g, 20.3 mmol) in THF was added slowly. The mixture was stirred at −78° C. for 2 h and then warmed up to rt. After cooling again to 0° C. 50 mL of aqueous saturated ammonium chloride was added and the mixture was extracted with ethyl acetate (3×80 mL). The combined organic layers were washed with brine (100 mL), dried over anhydrous sodium sulfate and filtered. The solvent was evaporated in vacuo and the product was purified by flash chromatography eluting with ethyl acetate/hexane (1:3) to afford the title compound as a solid (3.8 g, 59%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858785B2
Source datasetuspto-grants-2010_12
ORD IDord-922aeeea72b54aa68cb735041201ddcd
Source noteuspto-grants-2010_12