4-Cyanobenzaldehyde → 4-(2-Methoxyethenyl)benzonitrile

HRID 4874

반응식

HRID 4874 반응식
[Cl-].[CH3:2][O:3][CH2:4][P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.[C:24]([C:26]1[CH:33]=[CH:32][C:29]([CH:30]=O)=[CH:28][CH:27]=1)#[N:25]>COC(C)(C)C>[CH3:2][O:3][CH:4]=[CH:30][C:29]1[CH:32]=[CH:33][C:26]([C:24]#[N:25])=[CH:27][CH:28]=1

참가 물질

4

반응물 2

HCID 660424-CyanobenzaldehydeHCID 2723798Methoxymethyl-triphenylphosphonium chloride

생성물 1

HCID 536603324-(2-Methoxyethenyl)benzonitrile

시약·촉매·용매 1

HCID 15413tert-Butyl methyl ether용매2회

실험 절차

A suspension of 37.2 g of methoxymethyl-triphenylphosphonium chloride in 250 ml of t-butyl methyl ether is treated at room temperature while gassing with argon with 13.4 g of potassium t-butylate and stirred for 1 hour. Subsequently, the reaction mixture is treated at about 20° C. with a mixture of 9.49 g of 4-cyanobenzaldehyde and 100 mol of t-butyl methyl ether and stirred for a further 1 hours. Thereafter, the reaction mixture is partitioned in diethyl ether/water. The aqueous phase is extracted several times with diethyl ether. The organic phases are washed with water, dried over magnesium sulfate, filtered and evaporated. Chromatographic purification of the resulting crude product on silica gel with petroleum ether and toluene/hexane (vol. 3:1) gives 4-(2-methoxyvinyl)benzonitrile.

후처리

  1. additionis treated at room temperature
  2. stirringstirred for a further 1 hours
  3. customThereafter, the reaction mixture is partitioned in diethyl ether/water
  4. extractionThe aqueous phase is extracted several times with diethyl ether
  5. washThe organic phases are washed with water
  6. dry with materialdried over magnesium sulfate
  7. filtrationfiltered
  8. customevaporated
  9. customChromatographic purification of the resulting crude product on silica gel with petroleum ether and toluene/hexane (vol. 3:1)

출처 및 근거

ORD 기록
ord-f5389a0b5ac54c3387a6aa94190a6c9c
출처 데이터셋
uspto-grants-1993_09
특허 번호
US05242619

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