p-Toluenesulfonic acid → 4-(1,3-Thiazol-2-yl)phenol
反応式
[OH:1][C:2]1[CH:10]=[CH:9][C:5]([C:6](=[S:8])[NH2:7])=[CH:4][CH:3]=1.Br[CH2:12][CH:13](OC)OC.CC1C=CC(S(O)(=O)=O)=CC=1>CCO>[OH:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]2[S:8][CH:12]=[CH:13][N:7]=2)=[CH:4][CH:3]=1参加物
5
実験手順
To a mixture of 4-hydroxybenzothioamide (30.64 g, 0.20 mol) and 2-bromo-1,1-dimethoxyethane (31.00 g, 0.20 mol) in EtOH (600 mL) was added 4-methylbenzenesulfonic acid (34.44 g, 0.20 mol) with stirring at rt. The reaction mixture was heated at 90° C. for 24 h, then cooled to rt and concentrated in vacuo. The mixture was diluted with H2O (200 mL), adjusted to pH 10 with saturated NaHCO3 aqueous solution and extracted with DCM (200 mL×3). The combined organic phases were concentrated in vacuo to give the title compound as s yellow solid (21.3 g, 60%).
後処理
- temperatureThe reaction mixture was heated at 90° C. for 24 h
- temperaturecooled to rt
- concentrationconcentrated in vacuo
- additionThe mixture was diluted with H2O (200 mL)
- extractionextracted with DCM (200 mL×3)
- concentrationThe combined organic phases were concentrated in vacuo
出典と根拠
- ORDレコード
- ord-18f547aa7dbd4e959f7a411db9b1cb6c
- 出典データセット
- uspto-grants-2016_09
- 特許番号
- US09434695B2
反応ノート
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