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Dimethyl 5-(hydroxymethyl)isophthalate → Dimethyl 5-formylisophthalate

HRID 587935
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인쇄 미리보기

반응식

HRID 587935 반응식
[OH:1][CH2:2][C:3]1[CH:4]=[C:5]([C:13]([O:15][CH3:16])=[O:14])[CH:6]=[C:7]([CH:12]=1)[C:8]([O:10][CH3:11])=[O:9]>C(Cl)Cl.O=[Mn]=O>[CH:2]([C:3]1[CH:12]=[C:7]([C:8]([O:10][CH3:11])=[O:9])[CH:6]=[C:5]([CH:4]=1)[C:13]([O:15][CH3:16])=[O:14])=[O:1]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 13907324Dimethyl 5-(hydroxymethyl)isophthalate

생성물 1

HCID 15183982Dimethyl 5-formylisophthalate

시약·촉매·용매 2

HCID 14801Manganese dioxide촉매2회HCID 6344Dichloromethane용매

실험 절차

To a solution of 3.15 g (14.1 mmol) of dimethyl 5-(hydroxymethyl)isophthalate (prepared as described in Dimick et al., J. Am. Chem. Soc. (1999) 121, No. 44, 10286-10296) in 60 mL of DCM was added 7.34 g (84.4 mmol) of MnO2. The mixture was stirred at reflux for about 16 h and an additional 3.5 g of MnO2 was added. Refluxing was continued for another 6 h and the mixture was cooled, filtered through celite and evaporated to give dimethyl 5-formylisophthalate as a white solid which was used subsequently without purification.

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후처리

  1. temperatureat reflux for about 16 h
  2. temperatureRefluxing
  3. temperaturethe mixture was cooled
  4. filtrationfiltered through celite
  5. customevaporated

출처 및 근거

ORD 기록
ord-55c2bff881f5483c9e30f898767e27a1
출처 데이터셋
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09227918B2

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