Water → HCID 59637737, Verbindung

HRID 1892019Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1892019
Br[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][C:7]([O:9][CH2:10][C:11]#[C:12][Si:13]([CH3:16])([CH3:15])[CH3:14])=[O:8].[K].[C:18]1(=[O:28])[NH:22][C:21](=[O:23])[C:20]2=[CH:24][CH:25]=[CH:26][CH:27]=[C:19]12.C(Cl)(Cl)Cl.O>CN(C=O)C>[C:18]1(=[O:28])[N:22]([CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][C:7]([O:9][CH2:10][C:11]#[C:12][Si:13]([CH3:16])([CH3:15])[CH3:14])=[O:8])[C:21](=[O:23])[C:20]2=[CH:24][CH:25]=[CH:26][CH:27]=[C:19]12

Komponenten

6

Versuchsvorschrift

3-(trimethylsilyl)prop-2-ynyl 6-bromohexanoate (0.606 g, 2 mmol, 1 eq.) was added to a solution of phthalimide potassium salt (0.4412 g, 2.4 mmol, 1.2 eq.) in 50 mL of DMF and stirred overnight under argon. CHCl3 was added to the solution flask and was transferred to a separatory funnel containing water. The aqueous layer was separated and twice extracted with CHCl3. The combined organic layers were twice extracted with water then the solvent was removed on a rotary evaporator. Remaining solvent was removed under high vacuum overnight to yield a brown oil.

Aufarbeitung

  1. customwas transferred to a separatory funnel
  2. customThe aqueous layer was separated
  3. extractiontwice extracted with CHCl3
  4. extractionThe combined organic layers were twice extracted with water
  5. customthe solvent was removed on a rotary evaporator
  6. customRemaining solvent was removed under high vacuum overnight
  7. customto yield a brown oil

Quellen und Nachweise

ORD-Eintrag
ord-1ca5145ce0074dfaa3e8a06dbd24ecd4
Quelldatensatz
uspto-grants-2013_08
Patentnummer
US08507572B2

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