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Diethylamine → HCID 19907465, 화합물

HRID 2371540
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HRID 2371540 반응식
Br[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.[CH2:21]([NH:23][CH2:24][CH3:25])[CH3:22]>C(O)C>[CH2:21]([N:23]([CH2:24][CH3:25])[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][N:23]([CH2:24][CH3:25])[CH2:21][CH3:22])=[CH:10][CH:9]=1)[CH3:22]
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참가 물질

4

반응물 2

HCID 8021DiethylamineHCID 19907341HCID 19907341, 화합물

생성물 1

HCID 19907465HCID 19907465, 화합물수율 91.6%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

First, 0.42 g of 1,4-bis(6-bromohexyl)benzene and 0.44 g of diethylamine were dissolved in 5 ml of absolute ethanol, and the mixture was refluxed for 2 hours. After removing the solvent under a reduced pressure and adding chloroform, the mixture was evaporated under a reduced pressure. The residue was acidified with 1N hydrochloric acid, washed with chloroform, alkalized with 10% sodium hydroxide, subjected to salting out, and extracted with total 80 ml of chloroform. The extract was washed with water and a saturated sodium chloride aqueous solution, dried over magnesium sulfate, and evaporated under a reduced pressure to obtain 0.37 g of the title compound as a pale yellow liquid.

후처리

  1. temperaturethe mixture was refluxed for 2 hours
  2. customAfter removing the solvent under a reduced pressure
  3. additionadding chloroform
  4. customthe mixture was evaporated under a reduced pressure
  5. washwashed with chloroform
  6. extractionextracted with total 80 ml of chloroform
  7. washThe extract was washed with water
  8. dry with materiala saturated sodium chloride aqueous solution, dried over magnesium sulfate
  9. customevaporated under a reduced pressure

출처 및 근거

ORD 기록
ord-6b0139fff1fa4e6d9e228333ea1fe081
출처 데이터셋
uspto-grants-1992_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05093370

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