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Sodium borohydride → 6-Methoxy-1-benzothiophene

HRID 507684
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 507684
[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]2[C:10](=O)[CH2:9][S:8][C:7]=2[CH:12]=1.[BH4-].[Na+]>CO.[OH-].[Na+]>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]2[CH:10]=[CH:9][S:8][C:7]=2[CH:12]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 2

HCID 4311764Sodium borohydrideHCID 121016256-Methoxybenzo[B]thiophen-3(2H)-one

Produkt 1

HCID 136342376-Methoxy-1-benzothiopheneAusbeute 66,1 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 887MethanolLösungsmittel2×HCID 14798Sodium HydroxideLösungsmittel2×

Versuchsvorschrift

6-Methoxybenzo[b]thiophen-3(2H)-one (1.4 g, 7.76 mmol) was dissolved in a mixture of methanol (18 mL) and 2.5 M sodium hydroxide (3 mL). The mixture was treated with sodium borohydride (0.589 g, 15 mmol) in 10 mL of methanol and 3 mL of 2.5 M sodium hydroxide. The reflux was heated to reflux for 1 h and then at 60° C. overnight. The reaction was cooled down to room temperature and the methanol removed in vacuo. The remaining aqueous layer was acidified to pH 4 with 1 N hydrochloric acid. The aqueous layer was extracted with ethyl acetate and washed with 1 N HCl. The organic layer was further washed with water, saturated sodium bicarbonate, water and brine. The organic layer was dried with sodium sulfate, concentrated and purified by flash chromatography usng a gradient of 20 to 50% ethyl acetate in hexanes to afford a clear oil (0.843 g).

Aufarbeitung

  1. temperatureThe reflux was heated
  2. temperatureto reflux for 1 h
  3. customat 60° C.
  4. customovernight
  5. customthe methanol removed in vacuo
  6. extractionThe aqueous layer was extracted with ethyl acetate
  7. washwashed with 1 N HCl
  8. washThe organic layer was further washed with water, saturated sodium bicarbonate, water and brine
  9. dry with materialThe organic layer was dried with sodium sulfate
  10. concentrationconcentrated
  11. custompurified by flash chromatography

Quellen und Nachweise

ORD-Eintrag
ord-79b1d4e6ffc8444688f13ea1be1bc5af
Quelldatensatz
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07786132B2

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