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Phosphorus oxychloride → HCID 21270439, 화합물

HRID 1194544
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HRID 1194544 반응식
O[C:2]1[C:7]([C:8]([O:10][CH2:11][CH3:12])=[O:9])=[CH:6][N:5]=[C:4]2[CH2:13][N:14]([C:16]([O:18][CH3:19])=[O:17])[CH2:15][C:3]=12.P(Cl)(Cl)([Cl:22])=O>>[Cl:22][C:2]1[C:7]([C:8]([O:10][CH2:11][CH3:12])=[O:9])=[CH:6][N:5]=[C:4]2[CH2:13][N:14]([C:16]([O:18][CH3:19])=[O:17])[CH2:15][C:3]=12
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 24813Phosphorus oxychlorideHCID 178469476HCID 178469476, 화합물

생성물 1

HCID 21270439HCID 21270439, 화합물

실험 절차

A mixture of 8.44 g of ethyl 4-hydroxy-5,7-dihydro-6-methoxycarbonylpyrrolo[3,4-b]pyridine-3-carboxylate and 50 ml of phosphorous oxychloride is refluxed for four hours, cooled to room temperature, and evaporated to dryness. The residue is taken up in methylene chloride, cooled by the addition of ice and basified with 10N sodium hydroxide. The layers are separated, and the aqueous phase is re-extracted with methylene chloride. The combined organic extract is dried, filtered, and evaporated to dryness to give ethyl 4-chloro-5,7-dihydro-6-methoxycarbonylpyrrolo[3,4-b]pyridine-3-carboxylate

후처리

  1. temperatureis refluxed for four hours
  2. customevaporated to dryness
  3. temperaturecooled by the addition of ice and basified with 10N sodium hydroxide
  4. customThe layers are separated
  • extractionthe aqueous phase is re-extracted with methylene chloride
  • extractionThe combined organic extract
  • customis dried
  • filtrationfiltered
  • customevaporated to dryness
  • 출처 및 근거

    ORD 기록
    ord-0dfdbdd26b0a4f51b5ce54718d19363e
    출처 데이터셋
    uspto-grants-1989_03
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04814450

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