HCID 21304210, compound → Phthalic Acid
Reaction equation
[C:1]([O:22]C(CCC=C(C)C)(C=C)C)(=[O:21])[C:2]1[C:3](=[CH:17][CH:18]=[CH:19][CH:20]=1)[C:4]([O:6]C(CCC=C(C)C)(C=C)C)=[O:5]>O1CCCC1.[Pd]>[C:1]([OH:22])(=[O:21])[C:2]1[C:3](=[CH:17][CH:18]=[CH:19][CH:20]=1)[C:4]([OH:6])=[O:5]Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
A solution of 10 g (22.8 mmol) dilinalyl phthalate (prepared by the procedure of Example 1) in 100 mL tetrahydrofuran was treated with 2 g palladium on charcoal catalyst and hydrogenated quickly at 40 psi. A small amount of cleavage gave some phthalic acid byproduct, so the mixture was chromatographed on silica gel to give 7.1 g (70% yield) of pure viscous liquid Compound 6, confirmed by its nmr spectrum.
Sources & evidence
- ORD record
- ord-3d617ff46c34489fa23131ff63992059
- Source dataset
- uspto-grants-1989_05
- Patent number
- US04827019
Reaction notes
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