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2-[2-(4-Bromophenyl)ethoxy]ethanol → HCID 13208939、化合物

HRID 2078424
ノート
印刷プレビュー

反応式

HRID 2078424 の反応式
Br[C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH2:9][O:10][CH2:11][CH2:12][OH:13])=[CH:4][CH:3]=1.[C:14]([Cu])#[N:15]>CN(C=O)C>[C:14]([C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH2:9][O:10][CH2:11][CH2:12][OH:13])=[CH:4][CH:3]=1)#[N:15]
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

4

反応物 2

HCID 691375802-[2-(4-Bromophenyl)ethoxy]ethanolHCID 178418546HCID 178418546、化合物

生成物 1

HCID 13208939HCID 13208939、化合物

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
145 °C

実験手順

To a solution of 2-[2-(4-bromophenyl)ethoxy]ethanol (10.8 g, 0.044 mol; see step (iii) above in DMF (100 mL), CuCN (7.8 g, 0.088 mol) was added and refluxed at 140 to 150° C. overnight. After removal of DMF by distillation, the reaction was quenched by the addition of water. Inorganic matter was removed by filtration and the aqueous layer was extracted with ethyl acetate (4×100 mL). The combined organic layers were washed with water and brine before being concentrated. The crude product was purified by column chromatography (silica gel: 60-120 mesh, petroleum ether:ethyl acetate (75:25) eluent). This yielded 4.3 g (51%) of the sub-title compound.

後処理

  1. additionwas added
  2. customAfter removal of DMF
  3. distillationby distillation
  4. customthe reaction was quenched by the addition of water
  5. customInorganic matter was removed by filtration
  6. extractionthe aqueous layer was extracted with ethyl acetate (4×100 mL)
  7. washThe combined organic layers were washed with water and brine
  8. concentrationbefore being concentrated
  9. customThe crude product was purified by column chromatography (silica gel: 60-120 mesh, petroleum ether:ethyl acetate (75:25) eluent)

出典と根拠

ORDレコード
ord-59c8650abae344b583af1331eaf069b7
出典データセット
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07928225B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート