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Aluminium lithium hydride → 1,2,3,3a,8,8a-Hexahydroindeno[1,2-c]pyrrole

HRID 546297
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HRID 546297 반응식
[C:1]1(=O)[CH:5]2[CH2:6][C:7]3[CH:8]=[CH:9][CH:10]=[CH:11][C:12]=3[CH:4]2[CH2:3][NH:2]1.[H-].[H-].[H-].[H-].[Li+].[Al+3]>C1COCC1>[CH2:1]1[NH:2][CH2:3][CH:4]2[C:12]3[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=3[CH2:6][CH:5]12
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참가 물질

4

반응물 2

HCID 21226445Aluminium lithium hydrideHCID 58598870HCID 58598870, 화합물

생성물 1

HCID 115791751,2,3,3a,8,8a-Hexahydroindeno[1,2-c]pyrrole

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

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온도
70 °C

실험 절차

A solution of 3,3a,8,8a-tetrahydro-2H-2-aza-cyclopenta[a]inden-1-one (1.5 g, 8.8 mmol) in THF (44 mL) was cannulated to a solution of LAH in THF (26.4 mL, 1.0 M solution in THF). The resulting solution was stirred for 4 hours at 70° C., then overnight at room temperature. The reaction was quenched via the stepwise addition of H2O (1 mL), aqueous NaOH (1 mL, 2.0 M solution), and H2O (3 mL). The resulting mixture was filtered through celite, the celite washed with warm MeOH (200 mL), and the filtrate concentrated to give the subtitle compound and its regioisomer, which were used without further purification. MS calculated for C11H13N+H: 160, observed: 160.

후처리

  1. customovernight
  2. customat room temperature
  3. customThe reaction was quenched via the stepwise addition of H2O (1 mL), aqueous NaOH (1 mL, 2.0 M solution), and H2O (3 mL)
  4. filtrationThe resulting mixture was filtered through celite
  5. washthe celite washed with warm MeOH (200 mL)
  6. concentrationthe filtrate concentrated

출처 및 근거

ORD 기록
ord-15414ee242a9451ca73bf8bbf170965f
출처 데이터셋
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07935830B2

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