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N-Methylpiperidine → HCID 19907440, 화합물

HRID 2371542
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HRID 2371542 반응식
[Br:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][C:8]1[CH:13]=[CH:12][C:11]([CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19]Br)=[CH:10][CH:9]=1.[CH3:21][N:22]1[CH2:27][CH2:26][CH2:25][CH2:24][CH2:23]1>C(O)C>[Br-:1].[Br-:1].[CH3:21][N+:22]1([CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][C:8]2[CH:13]=[CH:12][C:11]([CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][N+:22]3([CH3:21])[CH2:27][CH2:26][CH2:25][CH2:24][CH2:23]3)=[CH:10][CH:9]=2)[CH2:27][CH2:26][CH2:25][CH2:24][CH2:23]1
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참가 물질

4

반응물 2

HCID 12291N-MethylpiperidineHCID 19907341HCID 19907341, 화합물

생성물 1

HCID 19907440HCID 19907440, 화합물수율 59.9%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

First, 0.28 g of 1,4-bis(6-bromohexyl)benzene and 0.5 g of N-methylpiperidine were dissolved in 4 ml of absolute ethanol, and the mixture was refluxed for 2 hours and evaporated under a reduced pressure to remove the solvent. After adding acetone and then ethanol, the whole was allowed to stand in a freezer for 3 days. The resulting crystal was collected by filtration, washed with acetone and dried under a reduced pressure to obtain 0.125 g of the title compound as a colorless crystal.

후처리

  1. temperaturethe mixture was refluxed for 2 hours
  2. customevaporated under a reduced pressure
  3. customto remove the solvent
  4. additionAfter adding acetone
  5. filtrationThe resulting crystal was collected by filtration
  6. washwashed with acetone
  7. customdried under a reduced pressure

출처 및 근거

ORD 기록
ord-709f7c76a01f4fdd84751258a888e845
출처 데이터셋
uspto-grants-1992_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05093370

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