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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1282313Generated: October 29, 2026

2-(Trimethylsilyl)ethanol → Trimethylsilanylethyl 2-fluoro-4-iodobenzoate

https://huagongshe.com/reaction/1282313

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Trimethylsilyl)ethanolHCID 18013—
Reactant2-Fluoro-4-iodobenzoic acidHCID 2774516—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductTrimethylsilanylethyl 2-fluoro-4-iodobenzoateHCID 54147505—

Reaction Steps

To a solution of 115.5 mg (0.4 mmol) of 2-fluoro-4-iodobenzoic acid (Compound B) in 10 mL of dichloromethane (under a blanket of argon) was added 91.5 mg (0.5 mmol) of 1-(3-dimethylaminopropyl-3-ethyl carbodiimide hydrochloride) and 53 mg (0.4 mmol) of 4-dimethylaminopyridine. To this reaction mixture was added 0.16 ml (132 mg, 1.1 mmol) of 2-trimethylsilylethanol and the resultant mixture was allowed to stir at ambient temperature for 23 hours. The reaction mixture was extracted between ethyl ether and water and the layers were separated. The aqueous phase was washed with ethyl ether (2×50 mL) and the organic phases were combined. The combined organic phase was washed with brine, dried over MgSO4, filtered and concentrated in vacuo to a clear, colorless oil. Purification by flash chromatography (silica, 3% ethyl acetate in hexane) gave the title compound as a clear, colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06455701B1
Source datasetuspto-grants-2002_09
ORD IDord-7c4d88568bf543b7bcf5c38041f0da1f
Source noteuspto-grants-2002_09