Benzyl Alcohol → Benzyl 6-hydroxyhexanoate
反応式
[C:1]1(=[O:8])[O:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[CH2:9]([OH:16])[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1.O.C1(C)C=CC(S(O)(=O)=O)=CC=1>>[OH:8][CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][C:6]([O:16][CH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)=[O:7]参加物
4
反応条件
- 温度
- 100 °C
実験手順
A mixture of ε-caprolactone (a) (40 g), benzyl alcohol and p-toluenesulfonic acid monohydrate (0.7 g) was stirred at 100° C. for 16 hours. The reaction mixture was treated in the conventional manner and was distilled under reduced pressure (1 mmHg, 140°-154° C.) to give the title compound (b).
後処理
- additionThe reaction mixture was treated in the conventional manner
- distillationwas distilled under reduced pressure (1 mmHg, 140°-154° C.)
出典と根拠
- ORDレコード
- ord-8701ea7f45784dd9bbd5c83a8eb7bd79
- 出典データセット
- uspto-grants-1994_03
- 特許番号
- US05290811
反応ノート
読み込み中…