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

HRID 380492
ノート
印刷プレビュー

反応式

HRID 380492 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 3283
Diethyl Ether
溶媒
2 回

実験手順

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.

後処理

  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)

出典と根拠

ORDレコード
ord-887dd1f3c5de462d8d2507ea0868b756
出典データセット
uspto-grants-2001_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06303593B1

反応ノート

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