Hydrochloric Acid → 6-Methoxybenzo[b]thiophene-2-ethanol

HRID 275743

Reaktionsgleichung

Reaktionsgleichung von HRID 275743
C([Li])CCC.[CH3:6][O:7][C:8]1[CH:9]=[CH:10][C:11]2[CH:15]=[CH:14][S:13][C:12]=2[CH:16]=1.[CH2:17]1[O:19][CH2:18]1.Cl>O1CCCC1>[CH3:6][O:7][C:8]1[CH:9]=[CH:10][C:11]2[CH:15]=[C:14]([CH2:17][CH2:18][OH:19])[S:13][C:12]=2[CH:16]=1

Komponenten

6

Reaktionsbedingungen

Temperatur
-30 °C

Versuchsvorschrift

Butyl lithium (0.27 mol of a 2.5 M solution) was added dropwise to 6-methoxybenzo[b]thiophene [prepared analogous to the procedure described in J. Med. Chem. 1989, 32(12), 2548-2554] (0.25 mol) in tetrahydrofuran (1000 ml), stirred at −30° C. The mixture was stirred for 10 minutes at −30° C. Ethylene oxide (0.38 mol in 100 ml tetrahydrofuran) was added dropwise at −30° C. The mixture was allowed to warm to room temperature and stirred for 3 hours. The mixture was acidified with dilute HCl solution. The solvent was evaporated. The residue was diluted with water and this mixture was extracted with CH2Cl2. The separated organic layer was dried, filtered and the solvent evaporated. The residue was stirred in hexane, filtered off and dried, yielding 41.3 g of 6-methoxybenzo[b]thiophene-2-ethanol (interm. 2).

Aufarbeitung

  1. customprepared analogous to the procedure
  2. temperatureto warm to room temperature
  3. stirringstirred for 3 hours
  4. customThe solvent was evaporated
  5. additionThe residue was diluted with water
  6. extractionthis mixture was extracted with CH2Cl2
  7. customThe separated organic layer was dried
  8. filtrationfiltered
  9. customthe solvent evaporated
  10. stirringThe residue was stirred in hexane
  11. filtrationfiltered off
  12. customdried

Quellen und Nachweise

ORD-Eintrag
ord-4653e6bd356b45a5af963add539b691f
Quelldatensatz
uspto-grants-2002_03
Patentnummer
US06352999B1

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