反応式
[F:1][C:2]([F:12])([F:11])[C:3]1[CH:10]=[CH:9][C:6]([CH:7]=O)=[CH:5][CH:4]=1.[H][H]>C(O)(=O)C.[Pt]>[F:1][C:2]([F:11])([F:12])[C:3]1[CH:4]=[CH:5][C:6]([CH3:7])=[CH:9][CH:10]=1参加物
5
実験手順
4-Trifluoromethylbenzaldehyde (20.0 g) was dissolved in acetic acid (100 ml) and treated with hydrogen in the presence of platinum (0.5 g) at ambient temperature and pressure for 10 hours. The solution was filtered, poured into water (400 ml), basified by addition of aqueous sodium hydroxide solution (2 M), extracted with ether (3×100 ml). The combined extracts were washed with water (2×100 ml), dried over anhydrous magnesium sulphate, evaporated to dryness. The residue was distilled to give 4-trifluoromethyltoluene (14.3 g) b.p. 131°-132° C. as a colourless mobil liquid.
後処理
- filtrationThe solution was filtered
- additionpoured into water (400 ml)
- additionbasified by addition of aqueous sodium hydroxide solution (2 M)
- extractionextracted with ether (3×100 ml)
- washThe combined extracts were washed with water (2×100 ml)
- dry with materialdried over anhydrous magnesium sulphate
- customevaporated to dryness
- distillationThe residue was distilled
出典と根拠
- ORDレコード
- ord-0a022bef1b89428289817bea16278ad2
- 出典データセット
- uspto-grants-1993_04
- 特許番号
- US05206257
関連ノート
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