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Potassium Carbonate → 5-(2-Methoxyphenyl)-1,3-oxazole

HRID 1023876
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HRID 1023876 반응식
CO[C:3]1[CH:4]=[CH:5][C:6]([CH:9]=[O:10])=[CH:7][CH:8]=1.[C:11]([O-:14])([O-])=O.[K+].[K+].CC1C=CC(S([CH2:27][N+:28]#[C-:29])(=O)=O)=CC=1>CO>[CH3:11][O:14][C:7]1[CH:8]=[CH:3][CH:4]=[CH:5][C:6]=1[C:9]1[O:10][CH:29]=[N:28][CH:27]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 11430Potassium CarbonateHCID 312444-MethoxybenzaldehydeHCID 161915Tosylmethyl isocyanide

생성물 1

HCID 167406765-(2-Methoxyphenyl)-1,3-oxazole수율 83%

시약·촉매·용매 1

HCID 887Methanol용매2회

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온도
80 °C

실험 절차

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

To a solution of Anisaldehyde (2.0 mmol) in MeOH (5.0 mL), was added K2CO3 (2.2 mmol) and TOSMIC (1.10 mmol) and the reaction was allowed to stir at 80° C. in a sealed vial. After the reaction was over, the methanol was removed and the crude product was absorbed in silica gel and purified by column chromatography. The product was isolated in 83% yield as colorless oil. 1H NMR: 3.91 (s, 3H), 6.94 (d, 1H, J=8.4 Hz), 7.01 (t, 1H, J=7.6 Hz), 6.94 (t, 1H, J=8.4 Hz), 7.53 (s, 1H), 7.75 (d, 1H, J=8.0 Hz), 7.53 (s, 1H).

후처리

  1. customwas removed
  2. customthe crude product was absorbed in silica gel
  3. custompurified by column chromatography
  4. customThe product was isolated in 83% yield as colorless oil

출처 및 근거

ORD 기록
ord-1581a934d57c46999e44e8ed2b0100f0
출처 데이터셋
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08722720B2

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