Phosphorus tribromide → (3-Bromoprop-1-yn-1-yl)benzene

HRID 343459

Reaction equation

HRID 343459 reaction equation
P(Br)(Br)[Br:2].[C:5]1([C:11]#[C:12][CH2:13]O)[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1>C(OCC)C.N1C=CC=CC=1>[C:5]1([C:11]#[C:12][CH2:13][Br:2])[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1

Participants

5

Conditions

Temperature
40 °C

Procedure

Phosphorous tribromide (2.62 mL, 27.6 mmol) was added to a solution of 3-phenyl-2-propyn-1-ol (10.0 g, 76 mmol) and pyridine (0.14 mL, 1.77 mmol) in diethyl ether (22 mL) at a rate to maintain reflux. After addition, the mixture was heated at 40° C. for 2 h. The mixture was cooled and poured onto ice. The organic layer was separated and diluted with diethyl ether (100 mL), washed with saturated sodium bicarbonate (2×50 mL) and saturated sodium chloride (50 mL). The organic layer was dried (MgSO4), filtered and concentrated in vacuo to afford 1-phenyl-3-bromo-1-propyn (13.4 g, 90%).

Workup

  1. temperatureto maintain
  2. temperaturereflux
  3. additionAfter addition
  4. temperatureThe mixture was cooled
  5. additionpoured onto ice
  6. customThe organic layer was separated
  7. additiondiluted with diethyl ether (100 mL)
  8. washwashed with saturated sodium bicarbonate (2×50 mL) and saturated sodium chloride (50 mL)
  9. dry with materialThe organic layer was dried (MgSO4)
  10. filtrationfiltered
  11. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-1b73f819b48c415593e24e3e635f7cbd
Source dataset
uspto-grants-1999_01
Patent number
US05861428

Linked notes

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