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Imidazole → 2-Bromo-4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-4,5,6,7-tetrahydrobenzo[b]thiophene

HRID 2247668
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2247668
[Br:1][C:2]1[S:3][C:4]2[CH2:10][CH2:9][CH2:8][CH:7]([OH:11])[C:5]=2[CH:6]=1.N1C=CN=C1.[C:17]([Si:21]([CH3:24])([CH3:23])Cl)([CH3:20])([CH3:19])[CH3:18].O>CN(C)C=O>[Br:1][C:2]1[S:3][C:4]2[CH2:10][CH2:9][CH2:8][CH:7]([O:11][Si:21]([C:17]([CH3:20])([CH3:19])[CH3:18])([CH3:24])[CH3:23])[C:5]=2[CH:6]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 795ImidazoleHCID 962WaterHCID 28928tert-Butyldimethylsilyl chlorideHCID 68523939HCID 68523939, Verbindung

Produkt 1

HCID 685257462-Bromo-4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-4,5,6,7-tetrahydrobenzo[b]thiopheneAusbeute 91 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228
Dimethylformamide
Lösungsmittel

Versuchsvorschrift

To a solution of 2-bromo-4,5,6,7-tetrahydro-1-benzothiophen-4-ol (5.0 g, 21 mmol) that was obtained in Example 8 (8a) in N,N-dimethylformamide (30 ml) were added successively imidazole (2.9 g, 43 mmol) and t-butyldimethylchlorosilane (3.5 g, 24 mmol) with stirring, and the resulting mixture was stirred for 2 hours. After stirring, the reaction mixture was poured into water (50 ml) to quench the reaction and extracted with ether. The extract was washed with a saturated aqueous solution of sodium chloride and dried over magnesium sulfate. After filtration, the filtrate was evaporated in vacuo, and the crude product of the title compound thus obtained was purified by chromatography on a silica gel column using a mixed solvent of ethyl acetate and hexane (1:9) as the eluent to afford the title compound (6.8 g) in a yield of 91% as a colourless oily product.

Aufarbeitung

  1. stirringthe resulting mixture was stirred for 2 hours
  2. stirringAfter stirring
  3. customto quench
  4. customthe reaction
  5. extractionextracted with ether
  6. washThe extract was washed with a saturated aqueous solution of sodium chloride
  7. dry with materialdried over magnesium sulfate
  8. filtrationAfter filtration
  9. customthe filtrate was evaporated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-d0a15647a0f54a7a852039e3ffbb147f
Quelldatensatz
uspto-grants-2010_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07687491B2

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