Acetic Anhydride → 1,1-Cyclohexanediacetic Anhydride
反応式
[C:1]1([CH2:11][C:12]([OH:14])=[O:13])([CH2:7][C:8]([OH:10])=O)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.C(OC(=O)C)(=O)C>>[CH2:4]1[CH2:3][CH2:2][C:1]2([CH2:7][C:8](=[O:10])[O:14][C:12](=[O:13])[CH2:11]2)[CH2:6][CH2:5]1参加物
3
実験手順
To a 100-mL round-bottomed flask was added 1,1-cyclohexanediacetic acid (2.03 g, 9.99 mmol) and acetic anhydride (11.6 mL). The reaction mixture was held at reflux for 2 hours, and then cooled to room temperature. Volatiles were removed via vacuum distillation (0.1 Torr, 20°-60° C.). The resulting crude product was dried under vacuum (0.1 Torr) at 80° C. for 14 hours to yield the title compound as a white solid which was used without further purification (1.75 g, 96%).
後処理
- temperatureat reflux for 2 hours
- customVolatiles were removed via vacuum distillation (0.1 Torr, 20°-60° C.)
- dry with materialThe resulting crude product was dried under vacuum (0.1 Torr) at 80° C. for 14 hours
出典と根拠
- ORDレコード
- ord-e5fe71e025b64909bd0eacd70766ca18
- 出典データセット
- uspto-grants-1999_01
- 特許番号
- US05859047
反応ノート
読み込み中…