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4-Nitro-o-toluic acid → (2-Methyl-4-nitrophenyl)methanol

HRID 1946322
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인쇄 미리보기

반응식

HRID 1946322 반응식
[CH3:1][C:2]1[CH:10]=[C:9]([N+:11]([O-:13])=[O:12])[CH:8]=[CH:7][C:3]=1[C:4](O)=[O:5]>C1COCC1.CO>[CH3:1][C:2]1[CH:10]=[C:9]([N+:11]([O-:13])=[O:12])[CH:8]=[CH:7][C:3]=1[CH2:4][OH:5]
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참가 물질

4

반응물 1

HCID 747904-Nitro-o-toluic acid

생성물 1

HCID 21345674(2-Methyl-4-nitrophenyl)methanol수율 102.5%

시약·촉매·용매 2

HCID 887Methanol용매2회HCID 8028Tetrahydrofuran용매

반응 조건

온도
80 °C

실험 절차

To a solution of 2-methyl-4-nitrobenzoic acid (5 g, 27.6 mmol, Aldrich) in THF) (95 ml) was added dropwise 1.0 M borane-tetrahydrofuran complex (55 ml, 55.0 mmol, Aldrich) at ambient temperature under nitrogen. The resulting red solution was heated to 80° C. for 2 h. To the solution at ambient temperature was added methanol (30 ml) and then heated to 80° C. for 30 min. The solvent was evaporated in vacuo to leave a yellow oil. The residue was dissolved in methanol (80 ml) and the solvent evaporated in vacuo to leave (2-methyl-4-nitrophenyl)methanol as a yellow solid (4.73 g).

후처리

  1. temperatureheated to 80° C. for 30 min
  2. customThe solvent was evaporated in vacuo
  3. customto leave a yellow oil
  4. customthe solvent evaporated in vacuo

출처 및 근거

ORD 기록
ord-69eef8c823434e7eab2fc1205ed4ff8b
출처 데이터셋
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08399436B2

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