Tetrahydrofuran → (1-(Pyrrolidin-1-yl)cyclopropyl)methanol
반응식
[N:1]1([C:6]2([C:9](OCC)=[O:10])[CH2:8][CH2:7]2)[CH2:5][CH2:4][CH2:3][CH2:2]1.O1CCCC1.[H-].[Al+3].[Li+].[H-].[H-].[H-].[OH-].[Na+]>O>[N:1]1([C:6]2([CH2:9][OH:10])[CH2:8][CH2:7]2)[CH2:5][CH2:4][CH2:3][CH2:2]1참가 물질
6
실험 절차
20.5 g of the product obtained in Step 3 and 100 ml of tetrahydrofuran are poured, over 5 minutes, into a suspension containing 8.57 g of lithium aluminium hydride and 400 ml of tetrahydrofuran. The mixture is heated at reflux for 2 hours, cooled to 5° C. and hydrolysed by successive additions of 9 ml of water, 9 ml of 4N sodium hydroxide solution and then 27 ml of water. The aluminium compound is filtered off and rinsed with tetrahydroflran. The combined filtrates are concentrated to dryness, allowing the desired product to be obtained (liquid).
후처리
- temperatureThe mixture is heated
- temperatureat reflux for 2 hours
- filtrationThe aluminium compound is filtered off
- washrinsed with tetrahydroflran
- concentrationThe combined filtrates are concentrated to dryness
- customto be obtained (liquid)
출처 및 근거
- ORD 기록
- ord-9fa619de0f9a40589588bee84f4458b7
- 출처 데이터셋
- uspto-grants-2005_09
- 특허 번호
- US06943184B2
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