Methanol → 2-(3,5-difluorophenyl)-2-methoxyacetic acid

HRID 1071441Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1071441
[F:1][C:2]1[CH:3]=[C:4]([CH:7]=[C:8]([F:10])[CH:9]=1)[CH:5]=[O:6].[CH:11](Br)(Br)Br.[OH-:15].[K+].[CH3:17][OH:18]>O.[Cl-].[Na+].O>[F:1][C:2]1[CH:3]=[C:4]([CH:5]([O:6][CH3:11])[C:17]([OH:18])=[O:15])[CH:7]=[C:8]([F:10])[CH:9]=1

Komponenten

7

Versuchsvorschrift

The title compound was prepared according to the general procedure in Reeve, et al, J.A.C.S., 83:2755 (1961). A solution of 3,5-difluorobenzaldehyde (Aldrich) and bromoform (1.2 eq.) In methanol was cooled to −5° C. and treated dropwise with methanolic KOH. The reaction temperature was held below 6 C. during the addition. The mixture was slowly warmed to room temperature and stirred overnight. The suspension was diluted with water and 50% saturated aqueous brine. The mixture was extracted with ether, and the aqueous layer was acidified to a pH around 3.5 and extracted with ether. The latter organic phase was dried over sodium sulfate, filtered and concentrated. The crude acid was purified via flash chromatography eluting with 1:4:95 acetic acid/methanol/methylene chloride to give a white solid. 1H NMR (300 MHz. CDCl3) δ 11.36 (1H, bs), 7.05 (1H, m), 6.81 (2H, tt, J=2.4, 8.8 Hz), 4.77 (1H, s), 3.47 (3H, s)/C9H8F2O3 (MW=202.17); mass spectroscopy—202.

Aufarbeitung

  1. additionduring the addition
  2. extractionThe mixture was extracted with ether
  3. extractionextracted with ether
  4. dry with materialThe latter organic phase was dried over sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customThe crude acid was purified via flash chromatography
  8. washeluting with 1:4:95 acetic acid/methanol/methylene chloride
  9. customto give a white solid

Quellen und Nachweise

ORD-Eintrag
ord-288de7d8cb674814a79cdd328cf1ca4b
Quelldatensatz
uspto-grants-2005_06
Patentnummer
US06906056B2

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