Acetic Acid → 6-methoxymethoxy-3,4-dihydro-2,5,7,8-tetramethyl-2H-1-benzopyran-2-carboxylic acid

HRID 1608506

Reaktionsgleichung

Reaktionsgleichung von HRID 1608506
[OH:1][C:2]1[C:3]([CH3:18])=[C:4]([CH3:17])[C:5]2[O:10][C:9]([CH3:14])([C:11]([OH:13])=[O:12])[CH2:8][CH2:7][C:6]=2[C:15]=1[CH3:16].[CH3:19][O:20][CH2:21]Br.C(O)(=O)C>N1C=CC=CC=1>[CH3:19][O:20][CH2:21][O:1][C:2]1[C:3]([CH3:18])=[C:4]([CH3:17])[C:5]2[O:10][C:9]([CH3:14])([C:11]([OH:13])=[O:12])[CH2:8][CH2:7][C:6]=2[C:15]=1[CH3:16]

Komponenten

5

Versuchsvorschrift

50 grams (0.2 mol) of 6-hydroxy-3,4-dihydro-2,5,7,8-tetramethyl-2H-1-benzopyran-2-carboxylic acid are dissolved in 150 cm3 of anhydrous pyridine. 16.34 cm3 (0.2 mol) of bromomethyl methyl ether are added dropwise. The mixture is stirred for 2 hours and then the solution is poured onto ice. The mixture is acidified with acetic acid and then extracted with methylene chloride. The organic phase is washed with water and dried over anhydrous sodium sulfate, then the title product is purified by passing through a column of silica gel, eluting with methylene chloride.

Aufarbeitung

  1. additionthe solution is poured onto ice
  2. extractionextracted with methylene chloride
  3. washThe organic phase is washed with water
  4. dry with materialdried over anhydrous sodium sulfate
  5. customthe title product is purified
  6. washeluting with methylene chloride

Quellen und Nachweise

ORD-Eintrag
ord-2275d5dcdb7b4a1b979b2779f63c64ca
Quelldatensatz
uspto-grants-1995_03
Patentnummer
US05395834

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