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Hydroxyamine hydrochloride → 1,2,3,3a,8,8a-Hexahydroindeno[1,2-c]pyrrole

HRID 1020315
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반응식

HRID 1020315 반응식
C([O-])(=O)C.[Na+].Cl.[NH2:7]O.[C:9]1(=O)[CH:12]2[CH2:13][C:14]3[CH:15]=[CH:16][CH:17]=[CH:18][C:19]=3[CH:11]2[CH2:10]1>CO>[CH2:9]1[NH:7][CH2:10][CH:11]2[C:19]3[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=3[CH2:13][CH:12]12
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참가 물질

5

반응물 3

HCID 443297Hydroxyamine hydrochlorideHCID 517045Sodium AcetateHCID 126384102,2a,7,7a-Tetrahydro-1H-cyclobuta[a]inden-1-one

생성물 1

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

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

Sodium acetate (1.45 g, 17.7 mmol) and hydroxylamine hydrochloride (0.68 g, 9.75 mmol) were added to a solution of 2,2a,7,7a-tetrahydro-cyclobuta[a]inden-1-one (1.4 g, 8.86 mmol) in MeOH (18 mL), and stirred overnight at room temperature. The reaction solution was concentrated via rotary evaporation. The residue was dissolved in CH2Cl2 (100 mL), washed with H2O (50 mL), dried over MgSO4, and concentrated to give the subtitle compound, which was used without further purification. MS calculated for C11H11NO+H: 174, observed: 174.

후처리

  1. concentrationThe reaction solution was concentrated via rotary evaporation
  2. dissolutionThe residue was dissolved in CH2Cl2 (100 mL)
  3. washwashed with H2O (50 mL)
  4. dry with materialdried over MgSO4
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-38a132b8f60f4901b066e54b9d87ad02
출처 데이터셋
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08716324B2

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