Chloromethyl Methyl Ether → Methyl 2-(methoxymethoxy)-4-methylbenzoate

HRID 37011

Reaktionsgleichung

Reaktionsgleichung von HRID 37011
[H-].[Na+].[CH3:3][C:4]1[CH:5]=[C:6]([OH:14])[C:7](=[CH:12][CH:13]=1)[C:8]([O:10][CH3:11])=[O:9].[CH3:15][O:16][CH2:17]Cl>CN(C)C=O.C(OCC)C>[CH3:15][O:16][CH2:17][O:14][C:6]1[CH:5]=[C:4]([CH3:3])[CH:13]=[CH:12][C:7]=1[C:8]([O:10][CH3:11])=[O:9]

Komponenten

6

Versuchsvorschrift

To a suspension of sodium hydride (1.62 g, 0.0675 mol) in 90 mL of dimethylformamide was added dropwise a solution of methyl 4-methylsalicylate (10.2 g, 0.0614 mol) in 20 mL of diethyl ether. After stirring for 15 minutes, a solution of chloromethyl methyl ether (5.6 mL, 0.0737 mol) in 10 mL of diethyl ether was added. The reaction mixture was stirred at room temperature for 18 hours and then it was partitioned between water and diethyl ether. The layers were separated and the aqueous layer was extracted an additional three times with diethyl ether. The combined organic extracts were washed with brine, dried with magnesium sulfate, and concentrated in vacuo to give 14.5 g of an oil. The product was purified by flash chromatography on silica gel eluting with 10%-15% ethyl acetate in hexane to give 9.41 g (73%) of product as an oil.

Aufarbeitung

  1. stirringThe reaction mixture was stirred at room temperature for 18 hours
  2. customit was partitioned between water and diethyl ether
  3. customThe layers were separated
  4. extractionthe aqueous layer was extracted an additional three times with diethyl ether
  5. washThe combined organic extracts were washed with brine
  6. dry with materialdried with magnesium sulfate
  7. concentrationconcentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-a932d15aa55b4939965179150bfcc5eb
Quelldatensatz
uspto-grants-1995_05
Patentnummer
US05418250

Verknüpfte Notizen

Wird geladen…