Reaktionsgleichung
[SH:1][C:2]1[CH:11]=[CH:10][C:5]([C:6]([O:8][CH3:9])=[O:7])=[CH:4][CH:3]=1.C(=O)([O-])[O-].[K+].[K+].Br[CH2:19][CH2:20][CH2:21][Cl:22]>CN(C)C=O>[Cl:22][CH2:21][CH2:20][CH2:19][S:1][C:2]1[CH:3]=[CH:4][C:5]([C:6]([O:8][CH3:9])=[O:7])=[CH:10][CH:11]=1Komponenten
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 60 °C
Versuchsvorschrift
To a solution of methyl 4-sulfanylbenzoate (2.00 g, 11.9 mmol) in N,N-dimethylformamide (13 mL) was added potassium carbonate (6.57 g, 47.6 mmol) and 1-bromo-3-chloro-propane (2.35 mL, 23.8 mmol). The mixture was heated at 60° C. for 16 h. The reaction mixture was filtered and the solvent removed in vacuo. The material was dissolved in dichloromethane (10 mL) and washed with water (3×10 mL) and a saturated aqueous NH4Cl (10 mL). The organic layer was dried over Na2SO4, filtered and the solvent removed in vacuo. Silica gel chromatography (0-100% dichloromethane/hexane) provided methyl 4-(3-chloropropylsulfanyl)benzoate (1.87 g, 64%) as a colorless viscous liquid. ESI-MS m/z calc. 244.0. Found 245.1 (M+1)+; Retention time: 1.83 minutes (3 min run). 1H NMR (400 MHz, DMSO-d6) δ 7.88 (d, J=8.5 Hz, 2H), 7.43 (d, J=8.2 Hz, 2H), 3.84 (s, 3H), 3.79-3.61 (m, 2H), 3.18 (t, J=7.2 Hz, 2H), 2.20-1.97 (m, 2H).
Aufarbeitung
- filtrationThe reaction mixture was filtered
- customthe solvent removed in vacuo
- dissolutionThe material was dissolved in dichloromethane (10 mL)
- washwashed with water (3×10 mL)
- dry with materialThe organic layer was dried over Na2SO4
- filtrationfiltered
- customthe solvent removed in vacuo
Quellen und Nachweise
- ORD-Eintrag
- ord-0381f2d4975d42e19823731662d0d9c7
- Quelldatensatz
- uspto-grants-2014_09
- Patentnummer
- US08828996B2
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