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Sodium Bicarbonate → 6-Ethenylpyridine-3-carbonitrile

HRID 1591195
ノート
印刷プレビュー

反応式

HRID 1591195 の反応式
[C:1]([C:3]1[CH:4]=[CH:5][C:6]([CH2:9][CH2:10]O)=[N:7][CH:8]=1)#[N:2].O.C1(C)C=CC(S(O)(=O)=O)=CC=1.C(=O)(O)[O-].[Na+]>C1(C)C=CC=CC=1>[C:1]([C:3]1[CH:4]=[CH:5][C:6]([CH:9]=[CH2:10])=[N:7][CH:8]=1)#[N:2]
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 516892Sodium BicarbonateHCID 521998p-Toluenesulfonic acid monohydrateHCID 19045350HCID 19045350、化合物

生成物 1

HCID 190453106-Ethenylpyridine-3-carbonitrile収率 36.3%

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

A mixture of 0.163 g (1.1 mmol) 5-cyano-2-(2-hydroxyethyl)pyridine and 0.029 g (0.15 mmol) p-toluenesulfonic acid hydrate in 10 mL toluene was heated to reflux for five hours in a flask equipped with a Dean-Stark trap. The cooled mixture was neutralized with 5 mL saturated sodium bicarbonate solution and extracted with ether (3×15 mL). The extract was washed with 3 mL brine, dried over sodium sulfate, and filtered. The filtrate was concentrated to give an oil which was purified by flash chromatography on silica gel elating with 1:3 ethyl acetate:hexane to give 0.052 g (36%) 5-cyano-2-vinylpyridine, mp 29°-30° C.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. temperaturewas heated
  2. temperatureto reflux for five hours in a flask
  3. customequipped with a Dean-Stark trap
  4. extractionextracted with ether (3×15 mL)
  5. washThe extract was washed with 3 mL brine
  6. dry with materialdried over sodium sulfate
  7. filtrationfiltered
  8. concentrationThe filtrate was concentrated
  9. customto give an oil which
  10. customwas purified by flash chromatography on silica gel elating with 1:3 ethyl acetate

出典と根拠

ORDレコード
ord-acc5f59fdc9b4c9eb2e7788c413f9372
出典データセット
uspto-grants-1993_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05206240

反応ノート

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