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Anthranilic Acid → Boc-2-Abz-OH

HRID 845377
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반응식

HRID 845377 반응식
[C:1]([OH:10])(=[O:9])[C:2]1[C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[NH2:4].C(=O)([O-])O[O:13][C:14]([CH3:17])([CH3:16])[CH3:15].CN([CH:23]=[O:24])C>>[C:23]([NH:4][C:3]1[C:2](=[CH:8][CH:7]=[CH:6][CH:5]=1)[C:1]([OH:10])=[O:9])([O:13][C:14]([CH3:15])([CH3:16])[CH3:17])=[O:24]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 227Anthranilic AcidHCID 6228DimethylformamideHCID 22251206HCID 22251206, 화합물

생성물 1

HCID 4087778Boc-2-Abz-OH

실험 절차

The pH value of a solution containing 4 g (30 mmoles) of anthranilic acid in 20 ml of DMF is adjusted to 8 by adding TEA. After adding 9 g of tertiary-butyloxy carbonate, the reaction mixture is stirred at room temperature overnight. The solvent is evaporated and the thick oily residue is dissolved in 50 ml of ethyl acetate. The organic phase is washed 3 times with 20 ml of ice-cold 0.01N sulfuric acid each, then 3 times with 20 ml of water each. The ethyl acetate solution is dried over anhydrous sodium sulfate and evaporated under reduced pressure. The thick oily residue becomes crystalline when kept in a refrigerator. The aimed product is obtained in a yield of 5.7 g (80%), m.p.: 91°-93° C.

후처리

  • additionby adding TEA
  • customThe solvent is evaporated
  • dissolutionthe thick oily residue is dissolved in 50 ml of ethyl acetate
  • washThe organic phase is washed 3 times with 20 ml of ice-cold 0.01N sulfuric acid each, then 3 times with 20 ml of water each
  • dry with materialThe ethyl acetate solution is dried over anhydrous sodium sulfate
  • customevaporated under reduced pressure
  • 출처 및 근거

    ORD 기록
    ord-4a22f0b8a8c94f40b9fc40f2da787f13
    출처 데이터셋
    uspto-grants-1988_07
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04758552

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