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4-Fluorophenol → 1-Benzyl-4-(2-(4-fluorophenoxy)ethyl)piperidine

HRID 380492
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HRID 380492 반응식
[CH2:1]([N:8]1[CH2:13][CH2:12][CH:11]([CH2:14][CH2:15][OH:16])[CH2:10][CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[F:17][C:18]1[CH:23]=[CH:22][C:21](O)=[CH:20][CH:19]=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.CCOC(/N=N/C(OCC)=O)=O>CCOCC>[CH2:1]([N:8]1[CH2:13][CH2:12][CH:11]([CH2:14][CH2:15][O:16][C:21]2[CH:22]=[CH:23][C:18]([F:17])=[CH:19][CH:20]=2)[CH2:10][CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 97324-FluorophenolHCID 11776TriphenylphosphineHCID 27250292-(1-Benzylpiperidin-4-yl)ethanolHCID 5462977Diethyl azodicarboxylate

생성물 1

HCID 99268361-Benzyl-4-(2-(4-fluorophenoxy)ethyl)piperidine수율 39.7%

시약·촉매·용매 1

HCID 3283
Diethyl Ether
용매
2회

실험 절차

To a solution of 1.5 g (6.84 mmol) of 1-benzyl-4-(2-hydroxy-1-ethyl)piperidine (Acros Chemical), 3.8 g (34.2 mmol) of 4-fluorophenol and 3.6 g (13.7 mmol) of triphenylphosphine in 25 mL of ether at 0° C. was slowly added dropwise 2.15 mL (13.7 mmol) of diethylazodicarboxylate (DEAD). The reaction mixture was allowed to warm to rt and was stirred for 12 h. To the reaction mixture was added 70 mL of ether and it was filtered through a thin pad of celite. The filtrate was washed with sat'd Na2CO3 solution and sat's NaCl solution. It was dried over MgSO4, filtered and the filtrate concentrated. The residue was purified by chromatography (silica, hexanes: ethyl acetate, 4:1) to give 0.85 g of the title compound.

후처리

  1. filtrationwas filtered through a thin pad of celite
  2. washThe filtrate was washed with sat'd Na2CO3 solution
  3. dry with materialIt was dried over MgSO4
  4. filtrationfiltered
  5. concentrationthe filtrate concentrated
  6. customThe residue was purified by chromatography (silica, hexanes: ethyl acetate, 4:1)

출처 및 근거

ORD 기록
ord-887dd1f3c5de462d8d2507ea0868b756
출처 데이터셋
uspto-grants-2001_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06303593B1

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