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4-Benzyl-2-(pyrrolidin-1-ylmethyl)morpholine → 2-(Pyrrolidin-1-ylmethyl)morpholine

HRID 2112765
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HRID 2112765 반응식
C([N:8]1[CH2:13][CH2:12][O:11][CH:10]([CH2:14][N:15]2[CH2:19][CH2:18][CH2:17][CH2:16]2)[CH2:9]1)C1C=CC=CC=1.[H][H]>C(O)C.[OH-].[Pd+2].[OH-].[C]>[N:15]1([CH2:14][CH:10]2[O:11][CH2:12][CH2:13][NH:8][CH2:9]2)[CH2:16][CH2:17][CH2:18][CH2:19]1
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참가 물질

5

반응물 2

HCID 230796524-Benzyl-2-(pyrrolidin-1-ylmethyl)morpholineHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 146275022-(Pyrrolidin-1-ylmethyl)morpholine수율 95%

시약·촉매·용매 2

HCID 178502593HCID 178502593, 화합물촉매HCID 702Ethanol용매

실험 절차

4-Benzyl-2-(pyrrolidin-1-ylmethyl)morpholine (450 mg, 1.73 mmol) prepared according to Process Step 1 was dissolved in ethanol (10 mL), and 20% palladium hydroxide-carbon (200 mg, 0.285 mmol) was suspended therein, followed by stirring under the hydrogen gas atmosphere for two days. Celite (registered trademark: 2.0 g) was suspended in the reaction mixture, the solid was separated by filtration, and the solvent was distilled off under reduced pressure from the filtrate. The residue was purified by silica gel column chromatography (chloroform:methanol=5:1) and thereby yielded 2-(pyrrolidin-1-ylmethyl)morpholine (280 mg, in a yield of 95%).

후처리

  1. customthe solid was separated by filtration
  2. distillationthe solvent was distilled off under reduced pressure from the filtrate
  3. customThe residue was purified by silica gel column chromatography (chloroform:methanol=5:1)

출처 및 근거

ORD 기록
ord-30b2270cd7874924b757e81fbc774dac
출처 데이터셋
uspto-grants-2009_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07524852B2

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