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2-Methoxybenzaldehyde → 5-(2-Methoxyphenyl)-1,3-oxazole

HRID 1581787
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인쇄 미리보기

반응식

HRID 1581787 반응식
[CH3:1][O:2][C:3]1[CH:10]=[CH:9][CH:8]=[CH:7][C:4]=1[CH:5]=[O:6].S([CH2:21][N+:22]#[C-:23])(C1C=CC(C)=CC=1)(=O)=O.C(=O)([O-])[O-].[K+].[K+]>CO>[CH3:1][O:2][C:3]1[CH:10]=[CH:9][CH:8]=[CH:7][C:4]=1[C:5]1[O:6][CH:23]=[N:22][CH:21]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 86582-MethoxybenzaldehydeHCID 11430Potassium CarbonateHCID 161915Tosylmethyl isocyanide

생성물 1

HCID 167406765-(2-Methoxyphenyl)-1,3-oxazole수율 70.4%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A mixture of 2-methoxybenzaldehyde (10.0 g, 73.4 mmol), tosylmethylisocyanide (14.34 g, 73.4 mmol) and potassium carbonate (10.14 g, 73.4 mmol) in 220 ml methanol is heated at reflux for 6 hours. The solvent is removed under reduced pressure and the residue poured into ice-water (800 ml). The precipitate is collected by filtration, washed with water, and dried in vacuo to give 9.05 g of 5-(2-methoxyphenyl)oxazole (70%).

후처리

  1. temperatureis heated
  2. temperatureat reflux for 6 hours
  3. customThe solvent is removed under reduced pressure
  4. additionthe residue poured into ice-water (800 ml)
  5. filtrationThe precipitate is collected by filtration
  6. washwashed with water
  7. customdried in vacuo

출처 및 근거

ORD 기록
ord-b811ba8842d64631a744eb5d9830d8f1
출처 데이터셋
uspto-grants-2004_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06730792B2

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