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Ethanol → Ethyl 4-bromo-6-methylpicolinate

HRID 1908810
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인쇄 미리보기

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HRID 1908810 반응식
[K+].[Br:2][C:3]1[CH:8]=[C:7]([CH3:9])[N:6]=[C:5]([C:10]([O-:12])=[O:11])[CH:4]=1.[CH2:13](O)[CH3:14]>OS(O)(=O)=O.C([O-])(O)=O.[Na+]>[CH2:13]([O:11][C:10]([C:5]1[CH:4]=[C:3]([Br:2])[CH:8]=[C:7]([CH3:9])[N:6]=1)=[O:12])[CH3:14]
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참가 물질

5

반응물 2

HCID 702EthanolHCID 67027109HCID 67027109, 화합물

생성물 1

HCID 25208981Ethyl 4-bromo-6-methylpicolinate

시약·촉매·용매 2

HCID 1118Sulfuric Acid용매HCID 516892Sodium Bicarbonate용매

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온도
70 °C

실험 절차

To a suspension of 4-bromo-6-methyl-pyridine-2-carboxylic acid potassium salt (253 mg, 0.996 mmol) in ethanol (100 mL), H2SO4 (2 mL) is added dropwise. The mixture is heated to 70° C. for 16 h before it is carefully diluted with sat. aq. NaHCO3. The mixture is extracted three times with diethyl ether. The combined org. extracts are dried over MgSO4, filtered and concentrated. The crude product is purified on prep. TLC plates with heptane:EA 3:2 to give 4-bromo-6-methyl-pyridine-2-carboxylic acid ethyl ester (105 mg) as a pale yellow oil; LC-MS: tR=0.85 min, [M+1]+=244.22.

후처리

  1. additionis added dropwise
  2. extractionThe mixture is extracted three times with diethyl ether
  3. dry with materialextracts are dried over MgSO4
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customThe crude product is purified on prep

출처 및 근거

ORD 기록
ord-206cfd363e164f28a5d5c20eddd7f3c9
출처 데이터셋
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08598208B2

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