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Toluene → 2-(Phenoxymethyl)piperidine

HRID 2186480
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HRID 2186480 반응식
[O:1]([CH2:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][N:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C1(C)C=CC=CC=1.CCOC(C)=O>C(O)(=O)C.C(Cl)Cl.[Pt]>[O:1]([CH2:8][CH:9]1[CH2:14][CH2:13][CH2:12][CH2:11][NH:10]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 3

HCID 1140TolueneHCID 8857Ethyl AcetateHCID 22456677HCID 22456677, 화합물

생성물 1

HCID 224566822-(Phenoxymethyl)piperidine

시약·촉매·용매 3

HCID 23939Platinum촉매HCID 176Acetic Acid용매HCID 6344Dichloromethane
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실험 절차

To a solution of 2-phenoxymethylpyridine (1.0 g, 5.4 mmol) in 23 mL of acetic acid was added 0.13 g of 5% Pt/C. The mixture was hydrogenated on a Parr shaker at 50 psi for 5 h. Toluene and EtOAc were added to the mixture and it was filtered and concentrated under reduced pressure to give an oil. The oil was dissolved in CH2Cl2 and washed with 10% NaOH. The organic layer was dried over Na2SO4, filtered and concentrated under reduced pressure to give a 50/50 mixture of the title compound and starting material as a yellow oil (1.0 g, 98%). ES (+) MS m/e=192 (M+H).

후처리

  1. filtrationwas filtered
  2. concentrationconcentrated under reduced pressure
  3. customto give an oil
  4. washwashed with 10% NaOH
  5. dry with materialThe organic layer was dried over Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure
  8. customto give

출처 및 근거

ORD 기록
ord-2dfd1e9386d64d5a8abf7a5c3e19bb1c
출처 데이터셋
uspto-grants-2002_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06403792B1

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