Hydrochloric Acid → 4-Hexyl-2-methoxy-1-phenoxybenzene

HRID 2246759

Reaktionsgleichung

Reaktionsgleichung von HRID 2246759
[CH2:1]([Mg]Cl)[CH2:2][CH2:3][CH2:4][CH2:5][CH3:6].Cl[C:10]1[CH:15]=[CH:14][C:13]([O:16][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)=[C:12]([O:23][CH3:24])[CH:11]=1.Cl>[Cl-].[Cl-].[Zn+2].CC(C)([P](C(C)(C)C)([Pd][P](C(C)(C)C)(C(C)(C)C)C(C)(C)C)C(C)(C)C)C.CN1CCCC1=O>[CH2:1]([C:10]1[CH:15]=[CH:14][C:13]([O:16][C:17]2[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=2)=[C:12]([O:23][CH3:24])[CH:11]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH3:6]

Komponenten

7

Versuchsvorschrift

Under nitrogen, ZnCl2 (0.5 M solution in tetrahydrofuran; 6.8 mL, 3.41 mmol) was added by syringe to a round-bottomed flask sealed with a rubber septum and purged with nitrogen. Hexyl magnesium chloride (1.0 M solution in THF; 4.0 mL, 4.26 mmol) was then added dropwise by syringe, and the resulting solution was stirred at room temperature for 20 minutes. Next, N-methylpyrrolidinone (4.7 mL) was added by syringe. After 5 minutes, 21.7 mg (0.0426 mmol) Pd(P(t-Bu)3)2 and 500 mg (2.13 mmol) of compound (3) were added. The flask was then fitted with a reflux condenser and heated under refluxed for 48 hours. The flask was then gradually cooled to room temperature, and 20 mL of a 1.0M aqueous HCl solution was added. The resulting mixture was extracted with diethyl ether and the ether extract was washed with water, then dried over anhydrous MgSO4 and concentrated under vacuum to give the crude product. Purification by flash chromatography on silica gel afforded analytically pure compound (4a): 1H NMR (300 MHz) (CDCl3): δ 7.36-6.80 (m, 8H), 3.90 (s, 3H), 2.71-2.66 (t, 2H), 1.74-1.67 (m, 2H), 1.42-1.33 (m, 6H), 1.01-0.97 (t, 3H).

Aufarbeitung

  1. customsealed with a rubber septum
  2. custompurged with nitrogen
  3. waitAfter 5 minutes
  4. customThe flask was then fitted with a reflux condenser
  5. temperatureheated
  6. temperatureunder refluxed for 48 hours
  7. temperatureThe flask was then gradually cooled to room temperature
  8. extractionThe resulting mixture was extracted with diethyl ether
  9. extractionthe ether extract
  10. washwas washed with water
  11. dry with materialdried over anhydrous MgSO4
  12. concentrationconcentrated under vacuum
  13. customto give the crude product
  14. customPurification by flash chromatography on silica gel

Quellen und Nachweise

ORD-Eintrag
ord-12a50118fbf5444c8e6902f424180700
Quelldatensatz
uspto-grants-2010_03
Patentnummer
US07687547B2

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