반응식
[C:1]([C:5]1[CH2:9][CH:8]=[C:7]([CH3:10])[CH:6]=1)([CH3:4])([CH3:3])[CH3:2].[CH3:11]C(C)=O.N1CCCC1.C(O[CH2:23][CH3:24])C>CO.O>[C:1]([C:5]1[CH:11]=[C:23]([CH3:24])[C:8](=[C:7]([CH3:6])[CH3:10])[CH:9]=1)([CH3:2])([CH3:3])[CH3:4]참가 물질
실험 절차
To a solution of 13.0 g (95.6 mmol) of 1-tert-butyl-3-methylcyclopentadiene in 130 ml of dehydrated methanol, 55.2 g (950.4 mmol) of dehydrated acetone was dropwise added in a nitrogen atmosphere at 0° C. with ice cooling, and 68.0 g (956.1 mmol) of pyrrolidine was further dropwise added, followed by stirring at room temperature for 4 days. After the reaction solution was diluted with 400 ml of diethyl ether, 400 ml of water was added. The organic phase was separated, washed with a 0.5N hydrochloric acid aqueous solution (150 ml×4), water (200 ml×3) and a saturated saline solution (150 ml), and then dried over anhydrous magnesium sulfate. The drying agent was filtered, and from the filtrate the solvent was distilled off to obtain a liquid. The liquid was subjected to vacuum distillation (70-80° C./0.1 mmHg) to obtain 10.5 g of a yellow liquid. The analyzed values are given below.
후처리
- additionwas further dropwise added
- additionwas added
- customThe organic phase was separated
- washwashed with a 0.5N hydrochloric acid aqueous solution (150 ml×4), water (200 ml×3)
- dry with materiala saturated saline solution (150 ml), and then dried over anhydrous magnesium sulfate
- filtrationThe drying agent was filtered
- distillationfrom the filtrate the solvent was distilled off
- customto obtain a liquid
- distillationThe liquid was subjected to vacuum distillation (70-80° C./0.1 mmHg)
출처 및 근거
- ORD 기록
- ord-0655bafe545c4163b57a20b2aaefd619
- 출처 데이터셋
- uspto-grants-2005_09
- 특허 번호
- US06939928B1
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