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

HRID 343021
ノート
印刷プレビュー

反応式

HRID 343021 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 (2.5M 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 (2M) 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 (2M) 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-c452759b32874dddacf6c5d05c3d5abd
出典データセット
uspto-grants-1999_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05859283

反応ノート

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