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Carbon Dioxide → 4-Chloro-2-fluoro-3-methylbenzoic acid

HRID 2256963
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HRID 2256963 반응식
C([Li])CCC.[Cl:6][C:7]1[CH:12]=[CH:11][CH:10]=[C:9]([F:13])[C:8]=1[CH3:14].[C:15](=[O:17])=[O:16]>O1CCCC1>[Cl:6][C:7]1[CH:12]=[CH:11][C:10]([C:15]([OH:17])=[O:16])=[C:9]([F:13])[C:8]=1[CH3:14]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 280Carbon DioxideHCID 99332-Chloro-6-fluorotolueneHCID 178418339Butyllithium

생성물 1

HCID 153137624-Chloro-2-fluoro-3-methylbenzoic acid

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

반응 조건

온도
-78 °C

실험 절차

n-Butyllithium (2.5 M in hexane, 100 ml) was added to a cooled solution of 2-chloro-6-fluorotoluene (36.1 g) in dry tetrahydrofuran while maintaining the temperature below -60° C. The mixture was stirred at -78° C. overnight then poured onto solid carbon dioxide pellets. The mixture was stirred and allowed to warm to room temperature. It was acidified to pH 1 and extracted with ether. The organic layer was extracted into aqueous sodium hydroxide solution (2 M) and water. The combined aqueous extracts were acidified to pH 1 and the solid formed was filtered off and washed with water and n-hexane to give 4-chloro-2-fluoro-3-methylbenzoic acid (40.35 g) as a white solid, NMR (DMSO-d6) 2.3(d,3H), 7.4(d,1H) 7.7(t,1H).

후처리

  1. temperaturewhile maintaining the temperature below -60° C
  2. stirringThe mixture was stirred
  3. temperatureto warm to room temperature
  4. extractionextracted with ether
  5. extractionThe organic layer was extracted into aqueous sodium hydroxide solution (2 M) and water
  6. customthe solid formed
  7. filtrationwas filtered off
  8. washwashed with water and n-hexane

출처 및 근거

ORD 기록
ord-15bd3650759f4b26992e3c1e1deeed7a
출처 데이터셋
uspto-grants-1997_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05656573

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