Water → 4'-Hydroxy-3-methyl-1,1'-biphenyl-4-carbonitrile

HRID 1167849

Reaktionsgleichung

Reaktionsgleichung von HRID 1167849
C[O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[CH:14]=[CH:13][C:12]([C:15]#[N:16])=[C:11]([CH3:17])[CH:10]=2)=[CH:5][CH:4]=1.B(Br)(Br)Br.O>C(Cl)Cl>[OH:2][C:3]1[CH:4]=[CH:5][C:6]([C:9]2[CH:14]=[CH:13][C:12]([C:15]#[N:16])=[C:11]([CH3:17])[CH:10]=2)=[CH:7][CH:8]=1

Komponenten

5

Versuchsvorschrift

The product from Example 164A (5.60 g, 25.4 mmol) in CH2Cl2 (120 mL) at 78° C. was treated with 1.0 M BBr3 (in CH2Cl2, 76 mL, 76.0 mmol) dropwise over 1 hour. After stirring for 14 hours at room temperature, the mixture was warmed to 0° C. (ice bath) and treated with water (0.5 mL). After 10 minutes, additional water was added (2.0 mL), ice bath was removed, and 5.0 mL of water was added. The mixture was then treated with another 20 mL of water and allowed to stir for 45 minutes. The mixture was filtered and the filtrate extracted with CH2Cl2. The CH2Cl2 layers were combined, dried over sodium sulfate, filtered, and the filtrate concentrated under reduced pressure to provide the title compound as an off-white powder (5.04 g, 94% yield). 1HNMR (300 MHz, CDCl3) δ2.35 (s, 3H), 5.0 (s, 1H), 6.79-7.50 (m, 7H); MS (DCI) m/z 210 (M+H)+.

Aufarbeitung

  1. temperaturethe mixture was warmed to 0° C. (ice bath)
  2. waitAfter 10 minutes
  3. customwas removed
  4. addition5.0 mL of water was added
  5. additionThe mixture was then treated with another 20 mL of water
  6. stirringto stir for 45 minutes
  7. filtrationThe mixture was filtered
  8. extractionthe filtrate extracted with CH2Cl2
  9. dry with materialdried over sodium sulfate
  10. filtrationfiltered
  11. concentrationthe filtrate concentrated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-504de1bbda9a4abd96557cbbaedfc2d0
Quelldatensatz
uspto-grants-2003_09
Patentnummer
US06620839B2

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