反応式
[Cl:1][C:2]([Cl:26])([Cl:25])[CH2:3][O:4][C:5](=[O:24])[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=1[CH2:12][S:13][C:14]1[CH:19]=[CH:18][CH:17]=[C:16](CC(O)=O)[CH:15]=1.SC1C=CC([CH2:34][C:35]([OH:37])=[O:36])=CC=1.ClC(Cl)(Cl)COC(=O)C1C=CC=CC=1CBr.C(=O)([O-])[O-].[Cs+].[Cs+]>CN(C=O)C>[Cl:26][C:2]([Cl:1])([Cl:25])[CH2:3][O:4][C:5](=[O:24])[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=1[CH2:12][S:13][C:14]1[CH:15]=[CH:16][C:17]([CH2:34][C:35]([OH:37])=[O:36])=[CH:18][CH:19]=1参加物
6
反応物 4
生成物 1
試薬・触媒・溶媒 1
実験手順
The titled compound was prepared according to the method described for 2-(3-carboxymethyl-phenylsulfanylmethyl)-benzoic acid 2,2,2-trichloro-ethyl ester above from 4-mercapto-phenylacetic acid (0.73 g, 4.33 mmol), 2-bromomethyl-benzoic acid 2,2,2-trichloro-ethyl ester (1.50 g, 4.33 mmol), cesium carbonate (1.69 g, 5.20 mmol) and DMF (25 mL). The crude material (1.88 g, 100%) was used for the next step without further purification; Mass spectrum: M−H+ 432.
後処理
- customThe crude material (1.88 g, 100%) was used for the next step without further purification
出典と根拠
- ORDレコード
- ord-4f1698b5de5d47e3a6e060f6f36c6888
- 出典データセット
- uspto-grants-2015_11
- 特許番号
- US09181181B2
関連ノート
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