Methanol → Methyl 4-tetrahydrofuran-3-ylsulfonylbenzoate
Reaktionsgleichung
[O:1]1[CH2:5][CH2:4][CH:3]([S:6][C:7]2[CH:16]=[CH:15][C:10]([C:11]([O:13][CH3:14])=[O:12])=[CH:9][CH:8]=2)[CH2:2]1.[OH2:17].OOS([O-])=O.[K+].C[OH:25]>>[O:1]1[CH2:5][CH2:4][CH:3]([S:6]([C:7]2[CH:8]=[CH:9][C:10]([C:11]([O:13][CH3:14])=[O:12])=[CH:15][CH:16]=2)(=[O:25])=[O:17])[CH2:2]1Komponenten
Versuchsvorschrift
Methyl 4-tetrahydrofuran-3-ylsulfanylbenzoate (1.01 g, 4.24 mmol) was dissolved in methanol (25 mL), followed by the addition of water (2.5 mL), and Oxone (2.61 g, 4.24 mmol). The reaction mixture was stirred at room temperature for 24 hours. An additional 0.1 eq of Oxone (0.26 g) was added and the reaction mixture was stirred for 2 hours, then filtered and the solvent was concentrated in vacuo. The resulting residue was dissolved in dichloromethane (30 mL) and washed with water (2×25 mL). The organic layer was dried over sodium sulfate, filtered and concentrated in vacuo to yield methyl 4-tetrahydrofuran-3-ylsulfonylbenzoate (1.07 g, 93%) as a yellow solid. ESI-MS m/z calc. 270.1. Found 271.3 (M+1)+; Retention time: 1.02 minutes (3 min run).
Aufarbeitung
- stirringthe reaction mixture was stirred for 2 hours
- filtrationfiltered
- concentrationthe solvent was concentrated in vacuo
- dissolutionThe resulting residue was dissolved in dichloromethane (30 mL)
- washwashed with water (2×25 mL)
- dry with materialThe organic layer was dried over sodium sulfate
- filtrationfiltered
- concentrationconcentrated in vacuo
Quellen und Nachweise
- ORD-Eintrag
- ord-bd4edeaafe1e4006afa71032eb83d489
- Quelldatensatz
- uspto-grants-2014_09
- Patentnummer
- US08828996B2
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