4-Bromo-2-ethylphenylboronic acid → HCID 178476529, 화합물

HRID 341698

반응식

HRID 341698 반응식
[C:1]([O-:4])(=[O:3])[CH3:2].[C:5]([O-:8])(=[O:7])[CH3:6].[C:9]([O-:12])(=[O:11])[CH3:10].C([O-])(=O)C.[Pb+4:17].[Br:18][C:19]1[CH:24]=[CH:23][C:22](B(O)O)=[C:21]([CH2:28][CH3:29])[CH:20]=1>>[C:1]([O-:4])(=[O:3])[CH3:2].[C:5]([O-:8])(=[O:7])[CH3:6].[C:9]([O-:12])(=[O:11])[CH3:10].[Br:18][C:19]1[CH:24]=[CH:23][C:22]([Pb+3:17])=[C:21]([CH2:28][CH3:29])[CH:20]=1

참가 물질

3

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온도
40 °C

실험 절차

To a mixture of lead tetraacetate (53 g, 0.12 mol) and mercuric diacetate (2.5 g, 0.0078 mol), thoroughly flushed with nitrogen, is added anhydrous chloroform (250 ml). This mixture is warmed to 40° C. and 4-bromo-2-ethylphenylboronic acid (25 g, 0.11 mol) is added in one portion and the mixture is stirred and heated at this temperature for 4 hours. After cooling to room temperature, cooled in an ice bath, filtered through a plug of diatomaceous earth and the filtrate is concentrated to approximately a quarter of its volume. Hexane is added to induce crystallization and the solvents evaporated under reduced pressure. Trituration with hexane gives 4-bromo-2-ethylphenyl lead triacetate (28 g).

후처리

  1. customthoroughly flushed with nitrogen
  2. additionis added anhydrous chloroform (250 ml)
  3. temperatureheated at this temperature for 4 hours
  4. temperatureAfter cooling to room temperature
  5. temperaturecooled in an ice bath
  6. filtrationfiltered through a plug of diatomaceous earth
  7. concentrationthe filtrate is concentrated to approximately a quarter of its volume
  8. additionHexane is added
  9. customcrystallization
  10. customthe solvents evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-66c96b4989b54d7cac56c093b825e16e
출처 데이터셋
uspto-grants-2014_11
특허 번호
US08895761B2

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