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Sodium Hydroxide → HCID 67314829, 화합물

HRID 1012576
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HRID 1012576 반응식
Cl.[C:2]([O:5][CH2:6][CH2:7][N:8]([CH2:20][C:21]1[CH:26]=[CH:25][C:24]([CH2:27][NH2:28])=[CH:23][CH:22]=1)[CH2:9][CH2:10][CH2:11][CH2:12][N:13]([CH2:17][CH2:18][CH3:19])[CH2:14][CH2:15][CH3:16])(=[O:4])[CH3:3].[OH-].[Na+]>O>[C:2]([O:5][CH2:6][CH2:7][N:8]([CH2:20][C:21]1[CH:26]=[CH:25][C:24]([CH2:27][NH2:28])=[CH:23][CH:22]=1)[CH2:9][CH2:10][CH2:11][CH2:12][N:13]([CH2:14][CH2:15][CH3:16])[CH2:17][CH2:18][CH3:19])(=[O:4])[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 67315568HCID 67315568, 화합물

생성물 1

HCID 67314829HCID 67314829, 화합물수율 99%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

5.8 g of the obtained [(4-aminomethylbenzyl)-(4-dipropylaminobutyl)amino]ethyl acetate hydrochloride (14a) was dissolved in 30 ml of water. After the addition of a 1N sodium hydroxide aqueous solution (pH=1), the mixture was extracted twice with 100 ml of chloroform. The chloroform layer was washed with 30 ml of water, dried over anhydrous sodium sulfate, and concentrated under reduced pressure, thereby obtaining 4.45 g of [(4-aminomethylbenzyl)-(4-dipropylaminobutyl)amino]ethyl acetate (14) as a colorless oily substance (yield: 99%, GC: 99.3%).

후처리

  1. extractionthe mixture was extracted twice with 100 ml of chloroform
  2. washThe chloroform layer was washed with 30 ml of water
  3. dry with materialdried over anhydrous sodium sulfate
  4. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-dc15c504e67a418e884571eec535096c
출처 데이터셋
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07977512B2

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