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

HRID 2256963
ノート
印刷プレビュー

反応式

HRID 2256963 の反応式
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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
-78 °C

実験手順

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).

後処理

  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

出典と根拠

ORDレコード
ord-15bd3650759f4b26992e3c1e1deeed7a
出典データセット
uspto-grants-1997_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05656573

反応ノート

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