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Methanol → Methyl 3-amino-5-chlorobenzoate

HRID 1801211
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HRID 1801211 반응식
[NH2:1][C:2]1[CH:3]=[C:4]([CH:8]=[C:9]([Cl:11])[CH:10]=1)[C:5]([OH:7])=[O:6].S(Cl)(Cl)=O.[CH3:16]O>>[CH3:16][O:6][C:5](=[O:7])[C:4]1[CH:8]=[C:9]([Cl:11])[CH:10]=[C:2]([NH2:1])[CH:3]=1
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참가 물질

4

반응물 3

HCID 887MethanolHCID 24386Thionyl ChlorideHCID 109867263-Amino-5-chlorobenzoic acid

생성물 1

HCID 52987785Methyl 3-amino-5-chlorobenzoate

실험 절차

To a stirred solution of 3-amino-5-chloro-benzoic acid (50 g, 291 mmol) in methanol (300 mL) was added thionyl chloride (45 mL, 605 mmol) dropewise at 0° C. Then the mixture solution was refluxed for 12 hours before cooling to room temperature. Then the reaction mixture was concentrated in vacuo and the residue was dissolved in ethyl acetate (500 mL), washed with saturated aqueous sodium bicarbonate solution (3×100 mL), dried over anhydrous sodium sulfate and concentrated in vacuo to afford 3-amino-5-chloro-benzoic acid methyl ester (54 g, quant.) as a pale-white solid: LC/MS m/e calcd for C8H8ClNO2 (M+H)+: 186.61, observed: 185.9.

후처리

  1. temperatureThen the mixture solution was refluxed for 12 hours
  2. concentrationThen the reaction mixture was concentrated in vacuo
  3. dissolutionthe residue was dissolved in ethyl acetate (500 mL)
  4. washwashed with saturated aqueous sodium bicarbonate solution (3×100 mL)
  5. dry with materialdried over anhydrous sodium sulfate
  6. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-2f0ceb59b9434c21b4af95af4f5e5229
출처 데이터셋
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08344137B2

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