Water → HCID 21180548, compound
Reaction equation
[OH-:1].[K+].[CH2:3]1[O:31][C:30]2[CH:29]=[CH:28][C:7]([O:8][C:9]3[CH:17]=[CH:16][CH:15]=[C:14]([O:18][C:19]4[CH:24]=[CH:23][C:22]5[O:25][CH2:26][O:27][C:21]=5[CH:20]=4)[C:10]=3[CH2:11][C:12]#N)=[CH:6][C:5]=2[O:4]1.[OH2:32]>C(O)C>[CH2:3]1[O:31][C:30]2[CH:29]=[CH:28][C:7]([O:8][C:9]3[CH:17]=[CH:16][CH:15]=[C:14]([O:18][C:19]4[CH:24]=[CH:23][C:22]5[O:25][CH2:26][O:27][C:21]=5[CH:20]=4)[C:10]=3[CH2:11][C:12]([OH:32])=[O:1])=[CH:6][C:5]=2[O:4]1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Potassium hydroxide (304 mg, 5.4 mmol) was added to a solution of 2,6-bis-[3,4-(methylenedioxy)phenoxy]benzyl cyanide (211 mg, 0.54 mmol) in ethanol (~5 ml) that had been dissolved in water (2 ml). The resulting suspension was then refluxed for 15 hours giving a pale yellow clear solution. The solvents were removed in vacuo and the remaining residue was dissolved in water. The aqueous solution was extracted with ethyl acetate (1×5 ml) to remove any unreacted starting material, and then the pH was adjusted to ~2.0 using concentrated HCl. The aqueous solution was then extracted into ethyl acetate and the organic phase was washed with brine (1×5 ml) and dried (MgSO4). Evaporation of solvents left a pale brown residue which was crystallized from MeOH/H2O to give 186 mg (81% yield) of the pure acid as a light tan colored solid (mp. 176-177° C.).
Workup
- temperatureThe resulting suspension was then refluxed for 15 hours
- customgiving a pale yellow clear solution
- customThe solvents were removed in vacuo
- dissolutionthe remaining residue was dissolved in water
- extractionThe aqueous solution was extracted with ethyl acetate (1×5 ml)
- customto remove
- extractionThe aqueous solution was then extracted into ethyl acetate
- washthe organic phase was washed with brine (1×5 ml)
- dry with materialdried (MgSO4)
- customEvaporation of solvents
- waitleft a pale brown residue which
- customwas crystallized from MeOH/H2O
Sources & evidence
- ORD record
- ord-d18fe21791f7477bb858265507682cd0
- Source dataset
- uspto-grants-1999_11
- Patent number
- US05977117
Reaction notes
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