Hexane → HCID 15238025, compound
Reaction equation
[C:1]([Br:5])(Br)(Br)[Br:2].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[CH:25]([CH2:27][CH:28]1[CH2:37][CH2:36][C:35]2[C:30](=[CH:31][CH:32]=[CH:33][C:34]=2[O:38][CH3:39])[CH2:29]1)=O.CCCCCC>C(Cl)Cl>[Br:2][C:1]([Br:5])=[CH:25][CH2:27][CH:28]1[CH2:37][CH2:36][C:35]2[C:30](=[CH:31][CH:32]=[CH:33][C:34]=2[O:38][CH3:39])[CH2:29]1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of carbon tetrabromide (19.5 g) in methylene chloride (50 ml) was added triphenylphosphine (30.8 g) at 0° C., and the mixture was stirred for 10 min. To the mixture was added a solution of 2-formylmethyl-5-methoxy-1,2,3,4-tetrahydronaphthalene (4.09 g; the compound prepared by method described in the specification of the Japanese Patent Application No. 3-130467) in methylene chloride (25 ml) at 0° C. The mixture was stirred for 30 min at 0° C. To the mixture was gradually added n-hexane, and filtrated to remove triphenylphosphineoxide. The filtrate was washed with water and a saturated aqueous solution of sodium chloride, successively, dried over anhydrous magnesium sulfate, and evaporated. The residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=24:1) to give the title compound (6.42 g) having the following physical data.
Workup
- customat 0° C
- stirringThe mixture was stirred for 30 min at 0° C
- filtrationfiltrated
- customto remove triphenylphosphineoxide
- washThe filtrate was washed with water
- dry with materiala saturated aqueous solution of sodium chloride, successively, dried over anhydrous magnesium sulfate
- customevaporated
- customThe residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=24:1)
Sources & evidence
- ORD record
- ord-50c2f8357316422f9b7edb4d3e5c5f6f
- Source dataset
- uspto-grants-1998_12
- Patent number
- US05849919
Reaction notes
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