Tetrahydrofuran → Isohexane ethyl acetate

HRID 1426874Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1426874
[C:1]([O:5][C:6]1[CH:7]=[C:8]([CH:19]=O)[C:9]2[S:13][C:12]([O:14][CH:15]([CH3:17])[CH3:16])=[N:11][C:10]=2[CH:18]=1)([CH3:4])([CH3:3])[CH3:2].[O:21]1[CH2:25][CH2:24][CH2:23][CH2:22]1>ClCCl>[C:1]([O:5][C:6]1[CH:7]=[C:8]([CH:19]=[CH2:22])[C:9]2[S:13][C:12]([O:14][CH:15]([CH3:16])[CH3:17])=[N:11][C:10]=2[CH:18]=1)([CH3:2])([CH3:3])[CH3:4].[C:22]([O:21][CH2:25][CH3:24])(=[O:5])[CH3:23].[CH3:18][CH2:6][CH2:7][CH:8]([CH3:19])[CH3:9]

Komponenten

5

Versuchsvorschrift

Ph3PMe.Br (5.0 g) is dissolved in dry tetrahydrofuran (100 ml) under argon. N-butyl lithium (8.8 ml, of 1.6 M solution) is added at room temperature over 10 minutes and reaction mixture stirred for a further 30 minutes. A solution of 5-tert-Butoxy-2-isopropoxy-benzothiazole-7-carbaldehyde (1.25 g) in dichloromethane (40 ml) is added drop wise to the reaction mixture and the reaction mixture is stirred for 4.5 hours at room temperature. The solvent is removed in vacuo, redissolved in ethyl acetate, washed with water (3×), brine (1×), dried over MgSO4, filtered and the solvent removed in vacuo. The title compound is obtained by flash column chromatography (silica, eluent ethyl acetate/iso-hexane 1:9).

Aufarbeitung

  1. customreaction mixture
  2. stirringthe reaction mixture is stirred for 4.5 hours at room temperature
  3. customThe solvent is removed in vacuo
  4. dissolutionredissolved in ethyl acetate
  5. washwashed with water (3×), brine (1×)
  6. dry with materialdried over MgSO4
  7. filtrationfiltered
  8. customthe solvent removed in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-651e16bd11614c2fa6d1de84314b8891
Quelldatensatz
uspto-grants-2015_01
Patentnummer
US08933108B2

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