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4-Benzyl-2-[4-(2-hydroxyethyl)-1-piperazinyl]methylmorpholine → 2-[4-(2-Hydroxyethyl)-1-piperazinyl]methylmorpholine

HRID 369886
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인쇄 미리보기

반응식

HRID 369886 반응식
C([N:8]1[CH2:13][CH2:12][O:11][CH:10]([CH2:14][N:15]2[CH2:20][CH2:19][N:18]([CH2:21][CH2:22][OH:23])[CH2:17][CH2:16]2)[CH2:9]1)C1C=CC=CC=1>C(O)C.[OH-].[Pd+2].[OH-]>[OH:23][CH2:22][CH2:21][N:18]1[CH2:19][CH2:20][N:15]([CH2:14][CH:10]2[O:11][CH2:12][CH2:13][NH:8][CH2:9]2)[CH2:16][CH2:17]1
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참가 물질

4

반응물 1

HCID 232826134-Benzyl-2-[4-(2-hydroxyethyl)-1-piperazinyl]methylmorpholine

생성물 1

HCID 232826232-[4-(2-Hydroxyethyl)-1-piperazinyl]methylmorpholine수율 79.1%

시약·촉매·용매 2

HCID 9942167Palladium hydroxide촉매HCID 702Ethanol용매

실험 절차

4-Benzyl-2-[4-(2-hydroxyethyl)-1-piperazinyl]methylmorpholine (16 g) is dissolved in ethanol (160 ml), and thereto is added palladium hydroxide (1.6 g). The mixture is subjected to de-benzylation at 50° C. under hydrogen atmosphere. Five hours later, the mixture is filtered through a cerite pad, and the filtrate is concentrated under reduced pressure. The resulting crystals are washed with diethyl ether-n-hexane to give 2-[4-(2-hydroxyethyl)-1-piperazinyl]methylmorpholine (9.09 g).

후처리

  1. customis subjected to de-benzylation at 50° C. under hydrogen atmosphere
  2. filtrationFive hours later, the mixture is filtered through a cerite pad
  3. concentrationthe filtrate is concentrated under reduced pressure
  4. washThe resulting crystals are washed with diethyl ether-n-hexane

출처 및 근거

ORD 기록
ord-e59bf8adeaee4e4aa9b9c56d5d124782
출처 데이터셋
uspto-grants-2000_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06140330

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