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Ammonium Chloride → 1-(2'-Methoxy-5'-fluorophenyl)pent-4-en-1-ol

HRID 1919508
ノート
印刷プレビュー

反応式

HRID 1919508 の反応式
[CH3:1][O:2][C:3]1[CH:10]=[CH:9][C:8]([F:11])=[CH:7][C:4]=1[CH:5]=[O:6].[CH:12]([Mg]Br)=[CH:13][CH2:14][CH3:15].[Cl-].[NH4+]>C1COCC1>[CH3:1][O:2][C:3]1[CH:10]=[CH:9][C:8]([F:11])=[CH:7][C:4]=1[CH:5]([OH:6])[CH2:15][CH2:14][CH:13]=[CH2:12]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 25517Ammonium ChlorideHCID 27349435-Fluoro-2-methoxybenzaldehydeHCID 178448305HCID 178448305、化合物

生成物 1

HCID 674998421-(2'-Methoxy-5'-fluorophenyl)pent-4-en-1-ol収率 93%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

To a solution of 2-methoxy-5-fluorobenzaldehyde (3.0 g, 19.5 mmol) in THF (20 mL) at 0° C. was added a solution 1-butenylmagnesium bromide (0.5 M in THF, 45 mL, 22.5 mmol) dropwise for 15 min. Then the reaction mixture was poured to a solution of saturated ammonium chloride (80 mL) in a separatory funnel. The organic fraction was extracted with ethyl acetate (3×60 mL) and the combined organic layers were washed with brine (50 mL) and dried over sodium sulfate. The solvent then was removed in vacuo and crude product thus obtained was purified by flash column chromatography (10% EtOAc in hexane, Rf=0.11) to give the product as an oil (3.27 g, 93%).

後処理

  1. extractionThe organic fraction was extracted with ethyl acetate (3×60 mL)
  2. washthe combined organic layers were washed with brine (50 mL)
  3. dry with materialdried over sodium sulfate
  4. customThe solvent then was removed in vacuo and crude product
  5. customthus obtained
  6. customwas purified by flash column chromatography (10% EtOAc in hexane, Rf=0.11)

出典と根拠

ORDレコード
ord-e0e94cea007a4d7d81192e362ff56e3c
出典データセット
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08168635B2

反応ノート

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