2-Methyl-2-butene → 1-(2-Bromopyridin-4-yl)cyclopropane-1-carboxylic acid

HRID 1423069노트

반응식

HRID 1423069 반응식
Cl([O-])=O.[Na+].[OH2:5].P([O-])(O)(O)=O.[Na+].[Br:12][C:13]1[CH:18]=[C:17]([C:19]2([CH:22]=[O:23])[CH2:21][CH2:20]2)[CH:16]=[CH:15][N:14]=1.CC(=CC)C>O.C(O)(C)(C)C>[Br:12][C:13]1[CH:18]=[C:17]([C:19]2([C:22]([OH:5])=[O:23])[CH2:20][CH2:21]2)[CH:16]=[CH:15][N:14]=1

참가 물질

7

반응물 4

HCID 105532-Methyl-2-buteneHCID 516949Sodium Phosphate, Monobasic, MonohydrateHCID 23668197Sodium ChloriteHCID 866727561-(2-Bromo-4-pyridinyl)cyclopropanecarboxaldehyde

생성물 1

HCID 717432461-(2-Bromopyridin-4-yl)cyclopropane-1-carboxylic acid

시약·촉매·용매 2

HCID 962Water용매HCID 6386tert-Butanol용매

실험 절차

A solution of sodium chlorite (368 mg, 3.26 mmol) and sodium dihydrogen phosphate monohydrate (449 mg, 3.26 mmol) in 5 mL of water is added dropwise to a solution of crude 1-(2-bromopyridin-4-yl)-cyclopropanecarboxaldehyde (566 mg, 2.50 mmol) and 2-methyl-2-butene (1.73 mL, 16.3 mmol) in t-butanol (12 mL), and the resulting reaction mixture is stirred at room temperature. After 18 hours, the mixture is concentrated in vacuo, acidified to pH 2 with 1 M aqueous HCl, diluted with brine (25 mL) and extracted with EtOAc (3×50 mL). The combined organic layers are dried over Na2SO4, filtered and concentrated to afford crude 1-(2-bromopyridin-4-yl)-cyclopropanecarboxylic acid which is used without purification.

후처리

  1. customthe resulting reaction mixture
  2. concentrationthe mixture is concentrated in vacuo
  3. additiondiluted with brine (25 mL)
  4. extractionextracted with EtOAc (3×50 mL)
  5. dry with materialThe combined organic layers are dried over Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated

출처 및 근거

ORD 기록
ord-2f52ecc95e7145a5b7755525fa9d037f
출처 데이터셋
uspto-grants-2015_01
특허 번호
US08927550B2

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