反応式
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]=1参加物
4
実験手順
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(3X), dried with MgSO4 and filtered and concentrated to give a white solid.
後処理
- 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(3X)
- dry with materialdried with MgSO4
- filtrationfiltered
- concentrationconcentrated
- customto give a white solid
出典と根拠
- ORDレコード
- ord-5efd89b5050f46a987a88ade1df59f7b
- 出典データセット
- uspto-grants-2006_08
- 特許番号
- US07098223B2
関連ノート
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