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2,4-Diisopropylphenol → 2-Bromo4,6-diisopropyl-phenol

HRID 2211129
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HRID 2211129 반응식
[Br:1]Br.[CH:3]([C:6]1[CH:11]=[C:10]([CH:12]([CH3:14])[CH3:13])[CH:9]=[CH:8][C:7]=1[OH:15])([CH3:5])[CH3:4]>C(O)(=O)C.[Fe]>[CH:3]([C:6]1[CH:11]=[C:10]([CH:12]([CH3:14])[CH3:13])[CH:9]=[C:8]([Br:1])[C:7]=1[OH:15])([CH3:5])[CH3:4]
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참가 물질

5

반응물 2

HCID 180482,4-DiisopropylphenolHCID 24408Bromine

생성물 1

HCID 145150292-Bromo4,6-diisopropyl-phenol수율 85.3%

시약·촉매·용매 2

HCID 23925Iron촉매HCID 176Acetic Acid용매

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온도
100 °C

실험 절차

1 g of iron powder and then, dropwise, 101 g (32.2 ml, 0.63 mol) of bromine are added in the course of 90 minutes to a solution of 102.3 g (0.57 mol) of 2,4-diisopropylphenol in 900 ml of glacial acetic acid at 95° C. The mixture is stirred for a further hour at 100° C. and cooled, the reaction mixture is partitioned between toluene and water and the toluene phase is washed with NaHCO3 solution. It is dried, filtered and concentrated, and the residue is distilled in a high vacuum. 125 g of the title compound is obtained as a pale yellow oil, b.p. 85° C./0.15 torr.

후처리

  1. temperaturecooled
  2. customthe reaction mixture is partitioned between toluene and water
  3. washthe toluene phase is washed with NaHCO3 solution
  4. customIt is dried
  5. filtrationfiltered
  6. concentrationconcentrated
  7. distillationthe residue is distilled in a high vacuum

출처 및 근거

ORD 기록
ord-a5ad9c6f24b141189df73cdebfef9dfa
출처 데이터셋
uspto-grants-1995_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05462933

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