HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 431694Generated: October 26, 2026
2-(Trimethylsilyl)ethanol → Trimethylsilanylethyl 2-fluoro-4-iodobenzoate
https://huagongshe.com/reaction/431694
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-(Trimethylsilyl)ethanol | HCID 18013 | — |
| Reactant | 2-Fluoro-4-iodobenzoic acid | HCID 2774516 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Trimethylsilanylethyl 2-fluoro-4-iodobenzoate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06660755B2 |
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| Source dataset | uspto-grants-2003_12 |
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| ORD ID | ord-0c4e45554f2a47ea83143b4db26ef270 |
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| Source note | uspto-grants-2003_12 |
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