Reaktion #367773

Reaktionsgleichung

water

Sodium hydride

3-hydroxypyridine

3-Bromomethylbenzo[b]thiophene-6-carboxylic acid methyl ester

→

3-(3-pyridyloxymethyl)benzo[b]thiophene-6-carboxylic acid methyl ester

Ausbeute 36.2%

Lösungsmittel

N,N-dimethylformamide

N,N-dimethylformamide

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.STIRRINGthe mixture was stirred at room temperature for 2 hours
2. 2
   ExtraktionThe mixture was extracted several times with ethyl acetate
3. 3
   Waschenthe combined extracts were washed with water
4. 4
   Trocknendried (Na2SO4)
5. 5
   SonstigeEvaporation of the solvent
6. 6
   Sonstigegave a gummy solid which
7. 7
   Sonstigewas chromatographed on silica gel
8. 8
   WaschenElution with chloroform
9. 9
   Sonstigefirst gave some impurity
10. 10
    SonstigeEvaporation of the product
11. 11
    workup.ADDITIONcontaining fractions

Vorschrift

Sodium hydride (0.12 g of 50% dispersion in mineral oil) was added to a solution of 3-hydroxypyridine (0.24 g) in dry N,N-dimethylformamide (5 ml) and the mixture was stirred for 30 minutes. 3-Bromomethylbenzo[b]thiophene-6-carboxylic acid methyl ester (0.71 g) in a small volume of N,N-dimethylformamide was added and the mixture was stirred at room temperature for 2 hours and then poured into water. The mixture was extracted several times with ethyl acetate and the combined extracts were washed with water and dried (Na2SO4). Evaporation of the solvent gave a gummy solid which was chromatographed on silica gel. Elution with chloroform first gave some impurity followed by pure product. Evaporation of the product containing fractions gave 3-(3-pyridyloxymethyl)benzo[b]thiophene-6-carboxylic acid methyl ester (0.27 g) which was used directly in the next stage.

Quelle