HCID 22341901, 화합물 → Acetyl-5-aminosalicylic acid

HRID 1787882노트

반응식

HRID 1787882 반응식
[C:1]([O:4][C:5]1[CH:13]=[CH:12][C:11]([NH:14]C(OC(C)(C)C)=O)=[CH:10][C:6]=1[C:7]([OH:9])=[O:8])(=[O:3])[CH3:2]>C(O)(C(F)(F)F)=O.C(Cl)Cl>[C:1]([O:4][C:5]1[CH:13]=[CH:12][C:11]([NH2:14])=[CH:10][C:6]=1[C:7]([OH:9])=[O:8])(=[O:3])[CH3:2]

참가 물질

3

반응물 1

HCID 22341901HCID 22341901, 화합물

생성물 1

HCID 13140652Acetyl-5-aminosalicylic acid수율 97.4%

시약·촉매·용매 1

HCID 21863450Trifluoroacetic acid methylene chloride용매

실험 절차

The mixture of 2-ethanoyloxy-5-tert-butoxycarbonylaminobenzoic acid (1.01 g, 3.42 mmole) in TFA/CH2Cl2 (20.0 ml. 1:1 v/v) was stirred for 30 min at room temperature. After the reaction mixture was concentrated, the residue was dissolved in ether. The resulting residue was recrystallized from ethyl acetate/hexane to give 0.65 g (97% yield) of 2-ethanoyloxy-5-aminobenzoic acid as a white solid.

후처리

  1. concentrationAfter the reaction mixture was concentrated
  2. dissolutionthe residue was dissolved in ether
  3. customThe resulting residue was recrystallized from ethyl acetate/hexane

출처 및 근거

ORD 기록
ord-f99c4245f5024eafbed92d5ba276e740
출처 데이터셋
uspto-grants-2009_03
특허 번호
US07511074B2

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