Pyridine → 131719-68-1

HRID 428961Notes

Reaction equation

HRID 428961 reaction equation
[CH:1]1(/[CH:7]=[CH:8]/[CH2:9]O)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.N1C=CC=CC=1.P(Br)(Br)[Br:18]>C(OCC)C>[Br:18][CH2:9]/[CH:8]=[CH:7]/[CH:1]1[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1

Participants

5

Procedure

To a stirred solution of (E)-3-cyclohexyl-2-propen-1-ol (A. G. M. Barrett et al, Tetrahedron, 1996, 52, 15325), (1.47 g, 10.5 mmol) in diethyl ether (20 ml) and pyridine (1 ml) was added phosphorus tribromide (1.40 ml, 15 mmol) dropwise at room temperature under an atmosphere of nitrogen. Afler 16 h, the reaction mixture was carefully poured onto ice water (100 ml) and extracted with diethyl ether (100 ml). The extract was washed with saturated aqueous sodium hydrogen carbonate solution (100 ml), dried (MgSO4) and concentrated in vacuo to give the crude product. This was purified by silica (20 g) column chromatography cluting with hexane:ethyl acetate (4:1) to give the title compound as a colourless oil (1.3 g, 61%).

Workup

  1. additionAfler 16 h, the reaction mixture was carefully poured onto ice water (100 ml)
  2. extractionextracted with diethyl ether (100 ml)
  3. washThe extract was washed with saturated aqueous sodium hydrogen carbonate solution (100 ml)
  4. dry with materialdried (MgSO4)
  5. concentrationconcentrated in vacuo
  6. customto give the crude product
  7. customThis was purified by silica (20 g) column chromatography

Sources & evidence

ORD record
ord-f19407caf4614eccb06575385f4b3683
Source dataset
uspto-grants-2001_11
Patent number
US06313312B1

Reaction notes

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