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Sodium Bicarbonate → 6-Ethenylpyridine-3-carbonitrile

HRID 1591195
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HRID 1591195 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 516892Sodium BicarbonateHCID 521998p-Toluenesulfonic acid monohydrateHCID 19045350HCID 19045350, 화합물

생성물 1

HCID 190453106-Ethenylpyridine-3-carbonitrile수율 36.3%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

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.

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후처리

  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

출처 및 근거

ORD 기록
ord-acc5f59fdc9b4c9eb2e7788c413f9372
출처 데이터셋
uspto-grants-1993_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05206240

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