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Methanol → 5-Fluoro-6-methylnicotinic acid

HRID 1810982
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HRID 1810982 반응식
C[O:2][C:3](=[O:12])[C:4]1[CH:9]=[C:8]([F:10])[C:7]([CH3:11])=[N:6][CH:5]=1.CO.[OH-].[Na+]>O>[F:10][C:8]1[C:7]([CH3:11])=[N:6][CH:5]=[C:4]([CH:9]=1)[C:3]([OH:12])=[O:2]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 887MethanolHCID 14798Sodium HydroxideHCID 57516328Methyl 5-Fluoro-6-methylnicotinate

생성물 1

HCID 575163295-Fluoro-6-methylnicotinic acid수율 88.4%

시약·촉매·용매 1

HCID 962Water용매

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온도
50 °C

실험 절차

To a suspension of 5-fluoro-6-methyl-nicotinic acid methyl ester (0.21 g, 1.24 mmol) in a 1:1 mixture of MeOH:water (20 mL) is added sodium hydroxide as a 10% aqueous solution (1.0 mL, 2.5 mmol). The mixture is heated to 50° C. for 1 h then cooled to room temperature and concentrated under reduced pressure to remove volatile organics. The pH of the resulting solution is adjusted to slightly acidic (approximately pH 5) by the addition of a 2N solution of HCl. The mixture is extracted with EtOAc and the combined organic phase is dried over anhydrous sodium sulfate and concentrated to provide 0.170 g of 5-fluoro-6-methyl-nicotinic acid as a solid.

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후처리

  1. temperaturethen cooled to room temperature
  2. concentrationconcentrated under reduced pressure
  3. customto remove volatile organics
  4. additionby the addition of a 2N solution of HCl
  5. extractionThe mixture is extracted with EtOAc
  6. dry with materialthe combined organic phase is dried over anhydrous sodium sulfate
  7. concentrationconcentrated

출처 및 근거

ORD 기록
ord-ad44ce75f6274c3c855db5834e44fef5
출처 데이터셋
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08362249B2

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