Sodium borohydride → (5,6-Dimethoxy-3-(4-methyloxyphenoxy)-benzo[b]thiophen-2-yl)methanol

HRID 1004124

Reaktionsgleichung

Reaktionsgleichung von HRID 1004124
[BH4-].[Na+].[CH3:3][O:4][C:5]1[C:24]([O:25][CH3:26])=[CH:23][C:8]2[S:9][C:10]([CH:21]=[O:22])=[C:11]([O:12][C:13]3[CH:18]=[CH:17][C:16]([O:19][CH3:20])=[CH:15][CH:14]=3)[C:7]=2[CH:6]=1>CO>[CH3:3][O:4][C:5]1[C:24]([O:25][CH3:26])=[CH:23][C:8]2[S:9][C:10]([CH2:21][OH:22])=[C:11]([O:12][C:13]3[CH:14]=[CH:15][C:16]([O:19][CH3:20])=[CH:17][CH:18]=3)[C:7]=2[CH:6]=1

Komponenten

4

Versuchsvorschrift

26 mmol of NaBH4 are added at room temperature to a solution of 24 mmol of the compound obtained in Step E of Example 1 in 100 ml of methanol. After 2 hours' reaction, one equivalent of NaBH4 is added to the reaction mixture. After 12 hours' reaction, the solution is concentrated and then diluted with ethyl acetate, washed with a 1N HCl solution, then with water and then with a saturated NaCl solution, subsequently dried over calcium sulphate, filtered and concentrated under reduced pressure. Chromatography over silica gel (dichloromethane/ethyl acetate: 95/5) enables 6.07 g of the expected product to be isolated.

Aufarbeitung

  1. additionis added to the reaction mixture
  2. customAfter 12 hours' reaction
  3. concentrationthe solution is concentrated
  4. additiondiluted with ethyl acetate
  5. washwashed with a 1N HCl solution
  6. dry with materialwith water and then with a saturated NaCl solution, subsequently dried over calcium sulphate
  7. filtrationfiltered
  8. concentrationconcentrated under reduced pressure
  9. customto be isolated

Quellen und Nachweise

ORD-Eintrag
ord-08dee4bf16114f4c80b7e9503bbda772
Quelldatensatz
uspto-grants-2000_04
Patentnummer
US06048875

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