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Acetic Anhydride → 3-(1-Acetoxytridecyl)-2-trimethylsilylfuran

HRID 1109908
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1109908
[CH2:1]([Mg]Br)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12].[CH3:15][Si:16]([CH3:25])([CH3:24])[C:17]1[O:18][CH:19]=[CH:20][C:21]=1[CH:22]=[O:23].[C:26](OC(=O)C)(=[O:28])[CH3:27]>O1CCCC1>[C:26]([O:23][CH:22]([C:21]1[CH:20]=[CH:19][O:18][C:17]=1[Si:16]([CH3:25])([CH3:24])[CH3:15])[CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12])(=[O:28])[CH3:27]
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Komponenten

5

Edukt 3

HCID 7918Acetic AnhydrideHCID 150371652-(Trimethylsilyl)furan-3-carbaldehydeHCID 178443215HCID 178443215, Verbindung

Produkt 1

HCID 150371423-(1-Acetoxytridecyl)-2-trimethylsilylfuran

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel2×

Versuchsvorschrift

Dodecylmagnesium bromide (a 1.0 M solution in tetrahydrofuran; 14.3 ml; 14.3 mmol) was added to a solution 2-trimethylsilyl-3-furaldehyde (1.20 g, 7.1 mmol) in tetrahydrofuran (20 ml). When all the aldehyde was consumed, as monitored by tlc, acetic anhydride (2.02 ml, 21.4 mmol) was added. Stirring was continued at room temperature for 14 hours. The mixture was quenched with water and was extracted with ethyl ether. Evaporation of the dried (magnesium sulfate) extracts gave an oil, which was purified by a silica column using 2% ethyl ether/hexane to give the titled furan.

Aufarbeitung

  1. customWhen all the aldehyde was consumed
  2. additionwas added
  3. customThe mixture was quenched with water
  4. extractionwas extracted with ethyl ether
  5. customEvaporation of the
  6. dry with materialdried (magnesium sulfate)
  7. customextracts gave an oil, which
  8. customwas purified by a silica column

Quellen und Nachweise

ORD-Eintrag
ord-d884a8e7e4c64a928bdea6a6e9cd76ba
Quelldatensatz
uspto-grants-1994_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05322953

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