Dimethylboronbromide → 1,1-Bis(2-hydroxyphenyl)cyclopropane

HRID 2165000Notes

Reaction equation

HRID 2165000 reaction equation
C[O:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[C:9]1([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=2[O:18]C)[CH2:11][CH2:10]1.BrB(C)C>ClCCl>[OH:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[C:9]1([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=2[OH:18])[CH2:11][CH2:10]1

Participants

4

Procedure

1,1-Bis(2-methoxyphenyl)cyclopropane (10.0 g, 0.039 mole) was combined with 60 ml of dichloromethane and the mixture was cooled in an ice bath and then treated with 10.0 ml of bromodimethylborane with cooling and stirring. The starting material was consumed in less than 1 hour as determined by gas-liquid chromatography. The mixture was then diluted with 500 ml of ether and the resulting solution was extracted twice with water and then with water saturated with ammonium chloride, dried over magnesium sulfate, filtered, and concentrated by evaporation under reduced pressure to obtain 9.0 g (101 percent of theory) of the title compound as a brownish-black solid: m.p., 158-160° C. This eluted as one clean peak in gas-liquid chromatography and had a proton NMR spectrum consistent with the assigned structure.

Workup

  1. temperaturethe mixture was cooled in an ice bath
  2. temperaturewith cooling
  3. customThe starting material was consumed in less than 1 hour
  4. additionThe mixture was then diluted with 500 ml of ether
  5. extractionthe resulting solution was extracted twice with water
  6. dry with materialwith water saturated with ammonium chloride, dried over magnesium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated by evaporation under reduced pressure

Sources & evidence

ORD record
ord-dd536669805649f487e51669f899c522
Source dataset
uspto-grants-1990_07
Patent number
US04938790

Reaction notes

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