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Water → 1-[2-(Benzyloxy)phenyl]ethan-1-one

HRID 1611118
ノート
印刷プレビュー

反応式

HRID 1611118 の反応式
[CH2:1]([O:8][C:9]1[C:10]([C:15]#N)=N[CH:12]=[CH:13][CH:14]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C[Mg]Br.O.S(=O)(=O)(O)O.[O:26]1CC[CH2:28][CH2:27]1>>[CH2:1]([O:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:15][C:10]=1[C:27](=[O:26])[CH3:28])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 5

HCID 962WaterHCID 1118Sulfuric AcidHCID 8028Tetrahydrofuran2 回HCID 222589533-(Benzyloxy)picolinonitrileHCID 178418573HCID 178418573、化合物

生成物 1

HCID 5205131-[2-(Benzyloxy)phenyl]ethan-1-one収率 92%

反応条件

温度
0 °C

実験手順

To a cold (0° C.) solution of 3-benzyloxypicolinonitrile (2.50 g, 11.9 mmol) in tetrahydrofuran (100 mL) was added dropwise 0.92M methyl magnesium bromide in tetrahydrofuran (150 mL, 138 mmol). The mixture was stirred at 0° C. for 30 minutes and then at room temperature for 4 hrs. The reaction mixture was poured into water (2000 mL) and acidified with 10% sulfuric acid (500 mL). After being stirred for 30 min, the reaction mixture was poured into saturate aqueous NaHCO3 solution slowly and extracted with ethyl acetate. The organic phase was washed with brine, dried over Na2SO4, filtrated, and evaporated. The residue was purified by column chromatography on silica gel (ethyl acetate/n-hexane=1/3) to give 1-(2-benzyloxyphenyl)-ethanone as a colorless oil (2.49 g, yield; 92%).

後処理

  1. waitat room temperature for 4 hrs
  2. stirringAfter being stirred for 30 min
  3. additionthe reaction mixture was poured
  4. concentrationinto saturate aqueous NaHCO3 solution slowly
  5. extractionextracted with ethyl acetate
  6. washThe organic phase was washed with brine
  7. dry with materialdried over Na2SO4
  8. filtrationfiltrated
  9. customevaporated
  10. customThe residue was purified by column chromatography on silica gel (ethyl acetate/n-hexane=1/3)

出典と根拠

ORDレコード
ord-3334d2ea47af4912bb1b0404acdcadd7
出典データセット
uspto-grants-2006_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06984649B1

反応ノート

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