Diethyl Ether → cis-Octahydroisoindole

HRID 53260

반응식

HRID 53260 반응식
C(OCC)C.[H-].[Al+3].[Li+].[H-].[H-].[H-].[C@@H:12]12[C:20](=O)[NH:19][C:18](=O)[C@@H:13]1[CH2:14][CH2:15][CH2:16][CH2:17]2.[OH-].[Na+]>O>[CH2:18]1[C@@H:13]2[C@@H:12]([CH2:17][CH2:16][CH2:15][CH2:14]2)[CH2:20][NH:19]1

참가 물질

6

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온도
0 °C

실험 절차

Cis-4-cyclohexene-1,2-dicarboximide (10.9 g) was hydrogenated over 10% palladium on carbon (1 g) in absolute ethanol (420 ml) at 50 psi for 10 minutes. The mixture was filtered then evaporated to give cis-cyclohexane-1,2-dicarboximide (10.6 g). To anhydrous diethyl ether (200 ml) was cannulated under nitrogen a 1M diethyl ether solution (200 ml) of lithium aluminium hydride. To the foregoing solution, under reflux, was added cis-cyclohexane-1,2-dicarboximide (10.6 g) portionwise over 10 minutes. The reaction mixture was heated to reflux for 3 hours. After cooling to 0° C., water (7 ml) was added followed by 4N sodium hydroxide (7.6 ml) and water (23 ml). The white suspension was stirred whilst warming to room temperature. The solid was removed by filtration then the filtrate dried (sodium sulphate) and evaporated to give a cream oil.

후처리

  1. temperatureTo the foregoing solution, under reflux
  2. temperatureThe reaction mixture was heated
  3. temperatureto reflux for 3 hours
  4. temperaturewhilst warming to room temperature
  5. customThe solid was removed by filtration
  6. dry with materialthe filtrate dried (sodium sulphate)
  7. customevaporated
  8. customto give a cream oil

출처 및 근거

ORD 기록
ord-6da0a4cd95cd436fb3bebd056b0cd0b4
출처 데이터셋
uspto-grants-1997_04
특허 번호
US05618812

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