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Carbon Dioxide → 2-Chloro-5-methylnicotinic acid

HRID 1827952
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HRID 1827952 반응식
C([Li])CCC.CCCCCC.CC1(C)CCCC(C)(C)N1.[Cl:22][C:23]1[CH:28]=[CH:27][C:26]([CH3:29])=[CH:25][N:24]=1.[C:30](=[O:32])=[O:31]>O1CCCC1>[Cl:22][C:23]1[N:24]=[CH:25][C:26]([CH3:29])=[CH:27][C:28]=1[C:30]([OH:32])=[O:31]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 5

HCID 280Carbon DioxideHCID 8058HexaneHCID 130352,2,6,6-TetramethylpiperidineHCID 5813932-Chloro-5-methyl-pyridineHCID 178418339Butyllithium

생성물 1

HCID 123877302-Chloro-5-methylnicotinic acid

시약·촉매·용매 1

HCID 8028
Tetrahydrofuran
용매

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온도
-78 °C

실험 절차

A 2.5M solution of butyllithium in hexane (9.4 mL, 23.5 mmol) was added to tetrahydrofuran (50 mL) and the mixture cooled to −78° C. The mixture was treated with 2,2,6,6-tetramethylpiperidine (4.4 mL, 26.0 mmol) and stirred at −78° C. for 30 minutes. The reaction mixture was then treated with 2-chloro-5-methylpyridine (3.00 g, 23.5 mmol) and stirred at −78° C. for a further 2.5 hours. The reaction mixture was poured into a beaker of dry ice and warmed to room temperature on a water bath, then extracted into water. The mixture was acidified with 2M hydrochloric acid, extracted into ether and washed with water (×2) and brine. The solution was dried over magnesium sulphate to yield the title product as a yellow solid, 1.65 g.

후처리

  1. stirringstirred at −78° C. for a further 2.5 hours
  2. temperaturewarmed to room temperature on a water bath
  3. extractionextracted into water
  4. extractionextracted into ether
  5. washwashed with water (×2) and brine
  6. dry with materialThe solution was dried over magnesium sulphate

출처 및 근거

ORD 기록
ord-1da7180b7edf4c748f56cd029cb1d0e8
출처 데이터셋
uspto-grants-2006_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07056934B2

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