Reaktionsgleichung
[CH3:1][CH:2]([CH2:6][CH3:7])[CH2:3][CH2:4][OH:5].[CH3:8][S:9](Cl)(=[O:11])=[O:10]>>[CH3:8][S:9]([O:5][CH2:4][CH2:3][CH:2]([CH3:1])[CH2:6][CH3:7])(=[O:11])=[O:10]Komponenten
3
Versuchsvorschrift
The title compound was prepared by following the general procedure of Example 43 for mesylation as a colorless oil (384 mg, 67%) from 3-methyl-1-pentanol (300 mg, 2.90 mmol) and methanesulfonyl chloride (500 mg, 4.40 mmol). 1H NMR (CDCl3, 300 MHz) δ0.86-0.95 (m, 6H), 1.15-1.25 (m, 1H), 1.33-1.42 (m, 1H), 1.51-1.60 (m, 2H), 1.76-1.84 (m, 1H), 3.00 (s, 3H), 4.23-4.31 (m, 2H) ppm.
Quellen und Nachweise
- ORD-Eintrag
- ord-e27cfb6552834923a9a940411aab37f9
- Quelldatensatz
- uspto-grants-2004_03
- Patentnummer
- US06713471B1
Verknüpfte Notizen
Wird geladen…