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Carbon Dioxide → 4-Bromopyridine-3-carboxylic acid

HRID 41617
ノート
印刷プレビュー

反応式

HRID 41617 の反応式
C([Li])CCC.C(NC(C)C)(C)C.Cl.[Br:14][C:15]1[CH:20]=[CH:19][N:18]=[CH:17][CH:16]=1.[C:21](=[O:23])=[O:22]>C1COCC1>[Br:14][C:15]1[C:20]([C:21]([OH:23])=[O:22])=[CH:19][N:18]=[CH:17][CH:16]=1
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

6

反応物 4

HCID 280Carbon DioxideHCID 7912DiisopropylamineHCID 881004-Bromopyridinium chlorideHCID 178418339Butyllithium

生成物 1

HCID 27629154-Bromopyridine-3-carboxylic acid

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
-55 °C

実験手順

Butyllithium (82.0 mL, 205.6 mmol, 2.0 eq.) was added dropwise to a solution of diisopropylamine (20.8 g, 205.6 mmol, 2.0 eq.) in THF (100 mL) at −78° C., under nitrogen. The resulting solution was stirred for 1 hour at approximately −60 to −50° C. The resulting solution was added dropwise to a solution of 4-bromopyridine hydrochloride (20.0 g, 102.9 mmol, 1.0 eq.) in THF (100 mL) at −78° C. The resulting solution was stirred for 2 hours. Carbon dioxide gas was introduced into the reaction vessel for 30 minutes. The resulting solution was stirred overnight at room temperature. The reaction was then quenched with water (100 mL). The resulting solution was extracted with EtOAc (3×200 mL) and the aqueous layers were combined. The pH of the solution was adjusted to 3-4 with 1N HCl to yield 4-bromonicotinic acid (16.8 g) as a white solid. ES m/z: [M+H]+ 202.

後処理

  1. stirringThe resulting solution was stirred for 2 hours
  2. stirringThe resulting solution was stirred overnight at room temperature
  3. customThe reaction was then quenched with water (100 mL)
  4. extractionThe resulting solution was extracted with EtOAc (3×200 mL)

出典と根拠

ORDレコード
ord-b08931e80e184f09b7e12c4e6de10b4b
出典データセット
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08530663B2

反応ノート

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