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Methanol → Methyl quinoline-3-carboxylate

HRID 587869
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인쇄 미리보기

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HRID 587869 반응식
[N:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[C:3]([C:11]([OH:13])=[O:12])[CH:2]=1.S(Cl)(Cl)=O.[CH3:18]O>>[N:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[C:3]([C:11]([O:13][CH3:18])=[O:12])[CH:2]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 887Methanol2회HCID 24386Thionyl ChlorideHCID 80971Quinoline-3-carboxylic acid

생성물 1

HCID 257955Methyl quinoline-3-carboxylate수율 99%

반응 조건

온도
80 °C

실험 절차

The solution of quinoline-3-carboxylic acid (3 g, 17.32 mmol) in methanol (30 mL) was cooled on ice bath at 0° C. Then thionyl chloride (1.264 mL, 17.32 mmol) was added and the reaction mixture was heated to 80° C. and maintained overnight. Reaction was monitored by TLC. After completion of reaction methanol was evaporated under reduced pressure and the resultant residue was basified with saturated sodium bicarbonate to make pH (7 to 8) to get white solid which was filtered and dried to get methyl quinoline-3-carboxylate (3.2 g, yield-99%) as a white solid; m/z-187.3.

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후처리

  1. temperaturemaintained overnight
  2. customReaction
  3. customwas evaporated under reduced pressure
  4. customto get white solid which
  5. filtrationwas filtered
  6. customdried

출처 및 근거

ORD 기록
ord-a56325cae9d242099af622a1cc532b81
출처 데이터셋
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09227919B2

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