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Carbon Dioxide → 4-Bromopyridine-3-carboxylic acid

HRID 41617
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HRID 41617 반응식
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
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참가 물질

6

반응물 4

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

생성물 1

HCID 27629154-Bromopyridine-3-carboxylic acid

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

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온도
-55 °C

실험 절차

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.

후처리

  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)

출처 및 근거

ORD 기록
ord-b08931e80e184f09b7e12c4e6de10b4b
출처 데이터셋
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08530663B2

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