Potassium Hydroxide → HCID 86733832, compound
Reaction equation
[C:1]12[CH2:7][C:4]([CH2:5][CH2:6]1)=[CH:3][CH:2]=2.C([CH:12]=[C:13]([C:17]#[N:18])[C:14]([OH:16])=[O:15])C(C)C.[OH-].[K+]>O>[C:1]12[CH2:7][C:4]([CH2:5][CH2:6]1)=[CH:3][CH:2]=2.[C:17]([C:13](=[CH2:12])[C:14]([OH:16])=[O:15])#[N:18]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Into a flask fitted with a condenser and magnetic stirring bar is charged 12.3 g (0.05 mole) norbornadiene/isobutyl 2-cyanoacrylic acid adduct and a solution of 4.9 g 86% potassium hydroxide (0.075 mole) in 75 ml. of water. After heating at reflux for 1.5 hours, the solution is cooled to room temperature and extracted with 2 × 25 ml. of hexane to remove any nonsaponified adduct. The aqueous phase is acidified to pH 2 with 6 N hydrochloric acid and the liberated oily product is taken up in 100 ml. ethyl acetate. The extract is filtered to remove some white insoluble solids (0.9 g., m.p. 182° C.) and the filtrate washed with 3 × 25 ml. water, 1 × 25 ml. saturated sodium chloride solution, and solvent stripped in vacuo to a pale yellow, viscous oil (8.7 g.). Crystallization of the oily product from benzene/hexane in the cold affords 4.2 g of the norbornadiene/2-cyanoacrylic acid adduct, white crystals, m.p. 83°-86° C. Another 3.0 g. of adduct, m.p. 81°-84° C., is obtained on concentration of the mother liquors and cooling. The combined crops and adduct are recrystallized from 1:2 benzene/hexane to afford 5.9 g of pure adduct, white crystals, m.p. 81°-83 ° C.
Workup
- customInto a flask fitted with a condenser and magnetic stirring bar
- temperatureAfter heating
- temperatureat reflux for 1.5 hours
- extractionextracted with 2 × 25 ml
- customof hexane to remove any nonsaponified adduct
- filtrationThe extract is filtered
- customto remove some white insoluble solids (0.9 g., m.p. 182° C.)
- washthe filtrate washed with 3 × 25 ml
- customCrystallization of the oily product from benzene/hexane in the
Sources & evidence
- ORD record
- ord-f9fc753bce4e434c920c54a9e06daa0d
- Source dataset
- uspto-grants-1977_03
- Patent number
- US04012402
Reaction notes
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