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methyl 2-[(E)-2-phenylvinyl]isonicotinate → Methyl 2-(2-cyclohexylethyl)piperidine-4-carboxylate

HRID 383917
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인쇄 미리보기

반응식

HRID 383917 반응식
[C:1]1(/[CH:7]=[CH:8]/[C:9]2[CH:10]=[C:11]([CH:16]=[CH:17][N:18]=2)[C:12]([O:14][CH3:15])=[O:13])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1>Cl.CO.[Pt]=O>[CH:1]1([CH2:7][CH2:8][CH:9]2[CH2:10][CH:11]([C:12]([O:14][CH3:15])=[O:13])[CH2:16][CH2:17][NH:18]2)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 1

HCID 59291512methyl 2-[(E)-2-phenylvinyl]isonicotinate

생성물 1

HCID 59291261Methyl 2-(2-cyclohexylethyl)piperidine-4-carboxylate

시약·촉매·용매 3

HCID 82844Platinum oxide (PtO)촉매HCID 313Hydrochloric Acid용매HCID 887Methanol용매

실험 절차

To a solution of methyl 2-[(E)-2-phenylvinyl]isonicotinate in hydrochloric acid and MeOH was added platinum oxide, followed by stirring at room temperature for 8 hours under a hydrogen atmosphere of 3 atm. The reaction mixture was filtered through Celite, and the filtrate was then concentrated under reduced pressure. To the residue were added an aqueous Na2CO3 solution and xylene, and the aqueous layer was extracted with CHCl3. The organic layer was dried over MgSO4 and then concentrated under reduced pressure to obtain methyl 2-(2-cyclohexylethyl)piperidine-4-carboxylate as a colorless oily substance.

후처리

  1. filtrationThe reaction mixture was filtered through Celite
  2. concentrationthe filtrate was then concentrated under reduced pressure
  3. additionTo the residue were added an aqueous Na2CO3 solution and xylene
  4. extractionthe aqueous layer was extracted with CHCl3
  5. dry with materialThe organic layer was dried over MgSO4
  6. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-cb895025838c4e5a974f502e8bd0dc88
출처 데이터셋
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08367696B2

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