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Nitric Acid → 2-Chloro-3-formyl-6-methoxy-5-nitrophenyl acetate

HRID 725352
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HRID 725352 반응식
[C:1]([O:4][C:5]1[C:10]([O:11][CH3:12])=[CH:9][CH:8]=[C:7]([CH:13]=[O:14])[C:6]=1[Cl:15])(=[O:3])[CH3:2].[N+:16]([O-])([OH:18])=[O:17]>>[C:1]([O:4][C:5]1[C:10]([O:11][CH3:12])=[C:9]([N+:16]([O-:18])=[O:17])[CH:8]=[C:7]([CH:13]=[O:14])[C:6]=1[Cl:15])(=[O:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 944Nitric AcidHCID 144509932-Chloro-3-formyl-6-methoxyphenyl acetate

생성물 1

HCID 144509942-Chloro-3-formyl-6-methoxy-5-nitrophenyl acetate

실험 절차

38 g of 2-chloro-3-formyl-6-methoxyphenyl acetate are introduced portionwise at -5° to -10° within 15 minutes into 150 ml of 98 percent nitric acid. After stirring at -5° for 30 minutes the reaction mixture is poured into 1.5 l of ice-water and extracted three times with 500 ml of methylene chloride. The combined organic phases are washed with ice-water, dried over sodium sulfate and evaporated. The residue is crystallized from ether. There is obtained 2-chloro-3-formyl-6-methoxy-5-nitrophenyl acetate of m.p. 84°-85°.

후처리

  1. extractionextracted three times with 500 ml of methylene chloride
  2. washThe combined organic phases are washed with ice-water
  3. dry with materialdried over sodium sulfate
  • customevaporated
  • customThe residue is crystallized from ether
  • 출처 및 근거

    ORD 기록
    ord-60ac0a04485e491b9c0c239126af4fa6
    출처 데이터셋
    uspto-grants-1998_01
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05705703

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