N-bromobutanimide → Ethyl 6-(bromomethyl)picolinate

HRID 2112995

반응식

HRID 2112995 반응식
[Br:1]N1C(=O)CCC1=O.[CH2:9]([O:11][C:12]([C:14]1[CH:19]=[CH:18][CH:17]=[C:16]([CH3:20])[N:15]=1)=[O:13])[CH3:10]>C(Cl)(Cl)(Cl)Cl.C(OOC(=O)C1C=CC=CC=1)(=O)C1C=CC=CC=1>[CH2:9]([O:11][C:12]([C:14]1[CH:19]=[CH:18][CH:17]=[C:16]([CH2:20][Br:1])[N:15]=1)=[O:13])[CH3:10]

참가 물질

5

반응물 2

HCID 67184N-bromobutanimide2회HCID 564597Ethyl 6-methylpyridine-2-carboxylate

생성물 1

HCID 23033755Ethyl 6-(bromomethyl)picolinate수율 32.2%

시약·촉매·용매 2

HCID 7187Benzoyl Peroxide촉매2회HCID 5943Carbon Tetrachloride용매

실험 절차

Finely ground N-bromo-succinimide (29.4 g, 165.2 mmol) was added in several portions to a solution of 6-methyl-pyridine-2-carboxylic acid ethyl ester (24.7 g, 150.0 mmol; available from Aldrich Chemical Company, Inc., Milwaukee, Wis.) in carbon tetrachloride (500 mL), and then benzoyl peroxide (100 mg, 0.4 mmol) was added. The mixture was heated at 84 degrees under nitrogen for approximately 40 h. Further portions of N-bromo-succinimide (14.8 g, 83.2 mmol) and then benzoyl peroxide (100 mg, 0.4 mmol) were added and heating was continued overnight. The reaction mixture was cooled to room temperature, filtered, evaporated, and purified by chromatography on silica gel using a Biotage system, eluting with 1:1 dichloromethane/hexane and dichloromethane to give 6-bromomethyl-pyridine-2-carboxylic acid ethyl ester (11.8 g, 32%) as a pale yellow oil. MS (MH+): 244/246. From HPLC, the purity was estimated at 85-90% and the material was used in the next step without further purification.

후처리

  1. temperatureThe mixture was heated at 84 degrees under nitrogen for approximately 40 h
  2. temperatureheating
  3. filtrationfiltered
  4. customevaporated
  5. custompurified by chromatography on silica gel using a Biotage system
  6. washeluting with 1:1 dichloromethane/hexane and dichloromethane

출처 및 근거

ORD 기록
ord-782978d24abb48a3b96654c63a9d5596
출처 데이터셋
uspto-grants-2009_04
특허 번호
US07524870B2

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