Reaktionsgleichung
C([O:8][C:9](=[O:24])[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=1[S:16][CH2:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)C1C=CC=CC=1.[OH-].[Na+].[OH-].[K+]>>[CH2:17]([S:16][C:11]1[CH:12]=[CH:13][CH:14]=[CH:15][C:10]=1[C:9]([OH:24])=[O:8])[C:18]1[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=1Komponenten
4
Versuchsvorschrift
To a suspension of 2-benzylsulfanyl benzoic acid benzyl ester 2 (113 mg, 0.34 mmol) was added 1.6 mL of 1N NaOH. KOH (1 pellet) was added and the reaction was continued overnight. The acetone was removed and a small amount of water was added. The aqueous solution was washed with CH2Cl2 (3×). The aqueous phase was acidified until pH of 2–3 was reached then extracted with CH2Cl2 (3×), dried with MgSO4 and filtered and concentrated to give a white solid.
Aufarbeitung
- customThe acetone was removed
- additiona small amount of water was added
- washThe aqueous solution was washed with CH2Cl2 (3×)
- extractionwas reached then extracted with CH2Cl2 (3×)
- dry with materialdried with MgSO4
- filtrationfiltered
- concentrationconcentrated
- customto give a white solid
Quellen und Nachweise
- ORD-Eintrag
- ord-baf0b29a82ef428887d0fd733df9acc0
- Quelldatensatz
- uspto-grants-2007_05
- Patentnummer
- US07214678B2
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