Phosphorus tribromide → 5-(2-bromoethyl)-2,3-dihydro-1H-indene

HRID 974974Notes

Reaction equation

HRID 974974 reaction equation
P(Br)(Br)[Br:2].O[CH2:6][CH2:7][C:8]1[CH:9]=[C:10]2[C:14](=[CH:15][CH:16]=1)[CH2:13][CH2:12][CH2:11]2>C(Cl)(Cl)(Cl)Cl>[Br:2][CH2:6][CH2:7][C:8]1[CH:9]=[C:10]2[C:14](=[CH:15][CH:16]=1)[CH2:13][CH2:12][CH2:11]2

Participants

4

Procedure

Phosphorus tribromide (3.5 ml) was added, dropwise, to a solution of 5-(2-hydroxyethyl)indane (14.0 g) (FR-A-2139628) in carbon tetrachloride (100 ml). The mixture was stirred at room temperature for 0.5 hour and then heated under reflux for 2 hours. Ice (100 g) was added and the-mixture partitioned between dichloromethane and 10% aqueous sodium carbonate. The layers were separated and the aqueous layer extracted with dichloromethane (2×100 ml). The combined dichloromethane extracts were dried (MgSO4) and concentrated in vacuo to give an oil which was purified by column chromatography on silica eluting with dichloromethane. The product-containing fractions were combined and concentrated in vacuo to give the title compound as a colourless oil, yield 10.5 g.

Workup

  1. temperatureheated
  2. temperatureunder reflux for 2 hours
  3. customthe-mixture partitioned between dichloromethane and 10% aqueous sodium carbonate
  4. customThe layers were separated
  5. extractionthe aqueous layer extracted with dichloromethane (2×100 ml)
  6. dry with materialThe combined dichloromethane extracts were dried (MgSO4)
  7. concentrationconcentrated in vacuo
  8. customto give an oil which
  9. customwas purified by column chromatography on silica eluting with dichloromethane
  10. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-985d13723bf844aeaec73143e7ee5deb
Source dataset
uspto-grants-1997_03
Patent number
US05607950

Reaction notes

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