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Acetic Acid → 2-(3-Bromobutyl)-3-methyl-6-nitrophenol

HRID 637627
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반응식

HRID 637627 반응식
C[CH:2]([C:5]1[C:10]([CH3:11])=[CH:9][CH:8]=[C:7]([N+:12]([O-:14])=[O:13])[C:6]=1[OH:15])[CH:3]=[CH2:4].[BrH:16].[C:17](O)(=O)C>>[Br:16][CH:4]([CH3:17])[CH2:3][CH2:2][C:5]1[C:10]([CH3:11])=[CH:9][CH:8]=[C:7]([N+:12]([O-:14])=[O:13])[C:6]=1[OH:15]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 176Acetic AcidHCID 260Hydrogen BromideHCID 202555762-(1-Methyl-2-propenyl)-3-methyl-6-nitrophenol

생성물 1

HCID 135602952-(3-Bromobutyl)-3-methyl-6-nitrophenol

반응 조건

온도
113 °C

실험 절차

A mixture of 155 ml of the crude 1B, 15 ml of glacial acetic acid and 135 ml of 48% hydrobromic acid was stirred at reflux (113° C.) for five hours, then concentrated at 30 Torr. and 80° C. for one hour. The residue was taken up in 500 ml of ether, dried (MgSO4), and filtered through Celite, and the solvent was evaporated from the filtrate. The residue was column-chromatographed on silica gel, using a 1:24 v:v mixture of THF and hexane as eluent. The product was recrystallized from ether/hexane to give 2-(3-bromobutyl)-3-methyl-6-nitrophenol (1C), as a light yellow solid, m.p.: 67°-69° C.

후처리

  1. concentrationconcentrated at 30 Torr
  2. dry with materialdried (MgSO4)
  3. filtrationfiltered through Celite
  4. customthe solvent was evaporated from the filtrate
  5. customThe residue was column-chromatographed on silica gel
  6. additionv mixture of THF and hexane as eluent
  7. customThe product was recrystallized from ether/hexane

출처 및 근거

ORD 기록
ord-4a2ace7de9414a52922d20376da7ea3a
출처 데이터셋
uspto-grants-1985_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04558040

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