Dimethylformamide → 2-Fluorobiphenyl-4-carboxaldehyde

HRID 874484

反応式

HRID 874484 の反応式
Br[C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)=[C:4]([F:14])[CH:3]=1.C([Li])CCC.CN([CH:23]=[O:24])C>O1CCCC1>[F:14][C:4]1[CH:3]=[C:2]([CH:23]=[O:24])[CH:7]=[CH:6][C:5]=1[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1

参加物

5

反応物 3

HCID 6228DimethylformamideHCID 5210634-Bromo-2-fluoro-1,1'-biphenylHCID 178418339Butyllithium

生成物 1

HCID 27590832-Fluorobiphenyl-4-carboxaldehyde収率 62.5%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

4-Bromo-2-fluoro-biphenyl (2 gm, 8 mmole) was dissolved in 20 ml of anhydrous tetrahydrofuran, THF, cooled to −78° C. under argon (Ar), n-Butyl lithium 2.5 M (3.5 ml, 8.8 mmole) was added drop wise over 10 min, and was stirred for additional 1 hr, DMF anhydrous (0.68 ml, 8.8 mmole) was then added, stirred for additional 1 hr, then warmed to room temperature over 4 hr, It was then quenched with water, extracted with ether, ether was dried, evaporated, the produced compound was purified using 9:1 hexane/ethyl acetate, to produce white solid (1 gm, 62.5%); H1-NMR INOVA-500 (CDCl3) δ 7.416-7.495 (m, 3H), 7.581-7.661 (m, 4H), 7.723 (d, J=8.0 Hz, 1H), 9.991 (s, 1H).

後処理

  1. stirringstirred for additional 1 hr
  2. customIt was then quenched with water
  3. extractionextracted with ether, ether
  4. customwas dried
  5. customevaporated
  6. customthe produced compound was purified

出典と根拠

ORDレコード
ord-b5189ec72d844b448fa59f85039f445b
出典データセット
uspto-grants-2015_03
特許番号
US08980890B2

関連ノート

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