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Ethyl orthoformate → Ethyl 2,3-dimethoxy-6-nitrobenzoate

HRID 979971
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HRID 979971 반응식
[CH3:1][O:2][C:3]1[C:11]([O:12][CH3:13])=[CH:10][CH:9]=[C:8]([N+:14]([O-:16])=[O:15])[C:4]=1[C:5]([OH:7])=[O:6].C(OCC)(OCC)O[CH2:19][CH3:20]>CN(C)C=O>[CH3:1][O:2][C:3]1[C:11]([O:12][CH3:13])=[CH:10][CH:9]=[C:8]([N+:14]([O-:16])=[O:15])[C:4]=1[C:5]([O:7][CH2:19][CH3:20])=[O:6]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 31214Ethyl orthoformateHCID 127623792,3-Dimethoxy-6-nitrobenzoic acid

생성물 1

HCID 13749913Ethyl 2,3-dimethoxy-6-nitrobenzoate

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

2,3-Dimethoxy-6-nitrobenzoic acid (l, 180.0 g, 0.792 mole) was dissolved in triethyl orthoformate (466.2 g, 3.14 mole) optionally containing dimethylformamide (4 mL) and the mixture was heated to reflux for one hour. The solvent was removed in vacuo, the residue was extracted with chloroform (2 L) and the organic layer was dried over magnesium sulfate. Removal of the solvent in vacuo gave the product as a pale brown oil which crystallized upon standing at room temperature, 202 g (100%, m.p. 70°-72° C.). This material could be recrystallized from isopropanol but was generally reacted in the next step without additional purification.

후처리

  1. temperaturethe mixture was heated
  2. temperatureto reflux for one hour
  3. customThe solvent was removed in vacuo
  4. extractionthe residue was extracted with chloroform (2 L)
  5. dry with materialthe organic layer was dried over magnesium sulfate
  6. customRemoval of the solvent in vacuo

출처 및 근거

ORD 기록
ord-52e3fec40c6949c9bc163cf01e8b9e2c
출처 데이터셋
uspto-grants-1987_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04634769

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