Allyl Alcohol → 2-(3-Hydroxypropyl)cyclododecanone
反応式
[C:1]1(=[O:13])[CH2:12][CH2:11][CH2:10][CH2:9][CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[CH2:14]([OH:17])[CH:15]=[CH2:16].C(OOC(C)(C)C)(C)(C)C>>[OH:17][CH2:14][CH2:15][CH2:16][CH:2]1[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][C:1]1=[O:13]参加物
4
実験手順
From a double-walled vessel made of glass, whose temperature is thermostatically controlled at 100° C. and which is fitted with a magnetic stirrer and serves as the storage container for the cyclododecanone, 400 g/h are pumped to a mixing column which is kept at a temperature of 100° C. 21.4 g/h of a mixture of allyl alcohol (12.2 g/h) and di-tert-butyl peroxide (9.2 g/h) are continuously metered into the feedline of the mixing column.
後処理
- customFrom a double-walled vessel made of glass, whose temperature
- customis thermostatically controlled at 100° C.
- customwhich is fitted with a magnetic stirrer
- customis kept at a temperature of 100° C
出典と根拠
- ORDレコード
- ord-abd32300fe634caea9c40bbcd4ac32fb
- 出典データセット
- uspto-grants-2001_04
- 特許番号
- US06222076B1
反応ノート
読み込み中…