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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507566Generated: November 3, 2026

Sodium Iodide → 2-(2-(4-Fluorobenzyl)thiophen-3-yl)ethanol

https://huagongshe.com/reaction/507566

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantSodium HydroxideHCID 14798—
Reactant(3-(2-(tert-Butyldimethylsilyloxy)ethyl)thiophen-2-yl)(4-fluorophenyl)methanolHCID 60204458—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product2-(2-(4-Fluorobenzyl)thiophen-3-yl)ethanolHCID 5742883075%

Reaction Conditions

Temperature0 °C

Reaction Steps

Chlorotrimethylsilane (5.56 g, 51.2 mmol) was added slowly to a solution of sodium iodide (7.7 g, 51.2 mmol) in acetonitrile (80 mL) at rt. After stirring for 15 min the mixture was cooled to 0° C. and a solution of (3-(2-(tert-butyldimethylsilyloxy)ethyl)thiophen-2-yl)(4-fluorophenyl)methanol (3.75 g, 10.2 mmol) in acetonitrile (10 mL) was added dropwise. The resulting mixture was stirred at 0° C. for 1 h and then at rt for 2 h. After cooling down to 0° C., 2 N sodium hydroxide (30 mL) was added slowly and the mixture stirred for 30 min. 100 mL of water 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 purified by flash chromatography eluting with ethyl acetate/hexane (1:20) to afford the title compound as a solid (1.8 g, 75%). MS (M+H)+ 237.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786132B2
Source datasetuspto-grants-2010_08
ORD IDord-ee15e185012c460283c1d7f8de5de45c
Source noteuspto-grants-2010_08