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2-Propylphenol → 4-Bromo-2-propylphenol

HRID 858609
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HRID 858609 반응식
[CH2:1]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[OH:10])[CH2:2][CH3:3].[Br-:11].[Br-].[Br-].C([N+](CCCC)(CCCC)CCCC)CCC.C([N+](CCCC)(CCCC)CCCC)CCC.C([N+](CCCC)(CCCC)CCCC)CCC>C(Cl)(Cl)Cl>[Br:11][C:8]1[CH:7]=[CH:6][C:5]([OH:10])=[C:4]([CH2:1][CH2:2][CH3:3])[CH:9]=1
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참가 물질

4

반응물 2

HCID 125702-PropylphenolHCID 23500184Tetra-n-butylammonium tribromide

생성물 1

HCID 221345104-Bromo-2-propylphenol

시약·촉매·용매 1

HCID 6212Chloroform용매2회

실험 절차

2-propylphenol (3.0 g, 0.022 mol) was dissolved in CHCl3 (100 mL) and magnetically stirred at room temperature. To this solution was added a solution of Tetrabutyl ammonium tribromide (10.68 g, 0.022 mol) in CHCl3 (100 mL). The resulting yellow solution was allowed to stir at room temperature for 1 hour. The reaction was quenched with a 5% solution of sodium thiosulfate (200 mL). The biphasic mixture was stirred for 15 min. The organics were separated and concentrated. The residue was dissolved in EtOAc (100 mL) and washed with water (2×100 mL) and brine (1×100 mL). The organics were dried over Na2SO4, filtered and concentrated. The residue was purified by flash chromatography (silica gel) eluting with 3% EtOAc in Hexanes. The result was a yellow oil (4.54 g).

후처리

  1. stirringto stir at room temperature for 1 hour
  2. customThe reaction was quenched with a 5% solution of sodium thiosulfate (200 mL)
  3. stirringThe biphasic mixture was stirred for 15 min
  4. customThe organics were separated
  5. concentrationconcentrated
  6. dissolutionThe residue was dissolved in EtOAc (100 mL)
  7. washwashed with water (2×100 mL) and brine (1×100 mL)
  8. dry with materialThe organics were dried over Na2SO4
  9. filtrationfiltered
  10. concentrationconcentrated
  11. customThe residue was purified by flash chromatography (silica gel)
  12. washeluting with 3% EtOAc in Hexanes

출처 및 근거

ORD 기록
ord-c7aef61e419f4af4b363fe7a32ded9ab
출처 데이터셋
uspto-grants-2006_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07148226B2

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