Ethanol → Ethyl-2-fluoro-4-iodo-phenyl acetate

HRID 427775Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 427775
FC([I:12])(C1C=CC=CC=1)C(O)=O.[F:13][C:14]1[CH:19]=[C:18](I)[CH:17]=[CH:16][C:15]=1[CH2:21][C:22](O)=O.S(=O)(=O)(O)O.[OH2:30].[CH2:31]([OH:33])[CH3:32]>C1C=CC=CC=1.CCCCCC.C(OCC)(=O)C>[C:31]([O:33][C:19]1[CH:18]=[CH:17][C:16]([I:12])=[C:15]([CH2:21][CH3:22])[C:14]=1[F:13])(=[O:30])[CH3:32]

Komponenten

9

Versuchsvorschrift

A solution of 2-fluoro-iodo-phenyl acetic acid (Intermediate 3, 1.75 g, 6.22 mmol) in ethanol (50 mL) and benzene (100 mL) was treated with concentrated sulfuric acid (1.4 mL) and heated at reflux overnight using a Dean-Stark water trap. The volatiles were distilled off in vacuo and the residue was diluted with water and diethyl ether. The phases were separated and the organic phase was washed with saturated aqueous sodium bicarbonate (×1), water (×1) and brine (×1), dried over anhydrous magnesium sulfate, filtered and evaporated in vacuo to afford an oil which was subjected to flash column chromatography over silica gel (230-400 mesh) using 5%-10% ethyl acetate in hexane as the eluent to afford the title compound as a pale yellow solid (1.4 g, 73%).

Aufarbeitung

  1. temperatureheated
  2. temperatureat reflux overnight
  3. distillationThe volatiles were distilled off in vacuo
  4. additionthe residue was diluted with water and diethyl ether
  5. customThe phases were separated
  6. washthe organic phase was washed with saturated aqueous sodium bicarbonate (×1), water (×1) and brine (×1)
  7. dry with materialdried over anhydrous magnesium sulfate
  8. filtrationfiltered
  9. customevaporated in vacuo
  10. customto afford an oil which

Quellen und Nachweise

ORD-Eintrag
ord-bc02f63da29846e4948dee9efe8d97e0
Quelldatensatz
uspto-grants-2001_11
Patentnummer
US06313107B1

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