Carbon Dioxide → 2,6-Difluoro-4-pentylbenzoic acid

HRID 466494ノート

反応式

HRID 466494 の反応式
C([Li])CCC.[F:6][C:7]1[CH:8]=[C:9]([CH2:14][CH2:15][CH2:16][CH2:17][CH3:18])[CH:10]=[C:11]([F:13])[CH:12]=1.[C:19](=[O:21])=[O:20].CCOCC>C1COCC1>[F:6][C:7]1[CH:8]=[C:9]([CH2:14][CH2:15][CH2:16][CH2:17][CH3:18])[CH:10]=[C:11]([F:13])[C:12]=1[C:19]([OH:21])=[O:20]

参加物

6

反応物 4

HCID 280Carbon DioxideHCID 3283Diethyl EtherHCID 157519781,3-Difluoro-5-pentylbenzeneHCID 178418339Butyllithium

生成物 1

HCID 190101792,6-Difluoro-4-pentylbenzoic acid

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

A solution of n-butyllithium (10.5M in hexane; 2.70 ml, 0.028 mol) was added dropwise to a stirred, cooled (-78° C.) solution of compound 13 (5.10 g, 0.028 mol) in dry THF (30 ml) under dry nitrogen. The stirred mixture was maintained under these conditions for 2.5 h and then poured onto a slurry of solid carbon dioxide and dry ether. The product was extracted into 10% sodium hydroxide which was then acidified with 36% hydrochloric acid. The acidic mixture was washed with ether (twice), and the combined ethereal layers were washed with water and dried (MgSO4). The solvent was removed in vacuo to yield a colourless solid.

後処理

  1. temperatureThe stirred mixture was maintained under these conditions for 2.5 h
  2. extractionThe product was extracted into 10% sodium hydroxide which
  3. washThe acidic mixture was washed with ether (twice), and the combined ethereal layers
  4. washwere washed with water
  5. dry with materialdried (MgSO4)
  6. customThe solvent was removed in vacuo
  7. customto yield a colourless solid

出典と根拠

ORDレコード
ord-eecfd88f3d4945319632e1940c5c7162
出典データセット
uspto-grants-1992_10
特許番号
US05156763

反応ノート

読み込み中…