反応式
[C:1]([CH:5]1[CH2:10][CH2:9][C:8](=O)[CH2:7][CH2:6]1)([CH3:4])([CH3:3])[CH3:2].[NH:12]1[CH2:16][CH2:15][CH2:14][CH2:13]1>C1(C)C=CC=CC=1>[C:1]([CH:5]1[CH2:10][CH2:9][C:8]([N:12]2[CH2:16][CH2:15][CH2:14][CH2:13]2)=[CH:7][CH2:6]1)([CH3:4])([CH3:3])[CH3:2]参加物
4
実験手順
A 50 mL round-bottomed flask containing 4-tert-butylcyclohexanone (6.01 gm) in anhydrous toluene (20 mL) was fitted with a Dean-Stark trap containing 3A molecular sieves, reflux condenser and a heating mantle. Pyrrolidine (6.00 mL) was added, and the solution heated to reflux for 18 hr. The solvent was evaporated and the crude product was used directly for the next reaction.
後処理
- customwas fitted with a Dean-Stark trap
- temperaturereflux condenser
- temperaturethe solution heated
- temperatureto reflux for 18 hr
- customThe solvent was evaporated
- customthe crude product was used directly for the next reaction
出典と根拠
- ORDレコード
- ord-bcf3b8f806d74b62bb2d057e7b5ce976
- 出典データセット
- uspto-grants-2015_12
- 特許番号
- US09216966B2
関連ノート
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