Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Reactant | Ethyl 3-cyano-5-methyl-3-hexenoate | HCID 85054034 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 53432669 | HCID 53432669 | — |
Reaction Steps
Ethyl 3-cyano-5-methylhex-3-enoate (mixture of E and Z isomers) and lithium hydroxide hydrate are suspended in a mixture of tetrahydrofuran and water. The slurry is vigorously stirred for 4 hours at room temperature. The mixture is acidified to pH 2 (3N HCl) and extracted into ethyl acetate (3×150 mL). The combined organic layers are dried (MgSO4), and the solvent is removed in vacuo to give crude 3-cyano-5-methylhex-3-enoic acid. The crude acid is dissolved in ethyl acetate (400 mL), and a solution of tert-butylamine in ethyl acetate (20 mL) is added. The temperature of the solution rises approximately 10° C. as a mass of white crystalline solid precipitates. The product is collected by filtration and dried in vacuo. Yield 22.15 g, 97.9 mmol, 89%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06891059B2 |
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| Source dataset | uspto-grants-2005_05 |
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| ORD ID | ord-647237047c1f41d68933fd006cbcaddd |
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| Source note | uspto-grants-2005_05 |
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