HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1297231Generated: October 31, 2026
Acetic Acid → Methyl 2-cyano-4-methylpent-2-enoate
https://huagongshe.com/reaction/1297231
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Isobutyraldehyde | HCID 6561 | — |
| Reactant | Methyl cyanoacetate | HCID 7747 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Methyl 2-cyano-4-methylpent-2-enoate | HCID 53793275 | — |
Reaction Steps
To a solution of isobutyraldehyde (18.2 mL, 200 mmol) in dry benzene (20 mL) was added methyl cyanoacetate (18 mL, 200 mmol), ammonium acetate (2 g) and glacial acetic acid (4 mL). The reaction mixture was' stirred at 60° C. for 30 minutes and allowed to cool to room temperature. Excess of solvents was removed in vacuo and the residue was dissolved in EtOAc (200 mL). The organic layer was washed with water, dried over sodium sulfate and evaporated to give 2-cyano-4-methyl-pent-2-enoic acid methyl ester as pale yellow oil. Further purification of the pale yellow oil by distillation (7 mm Hg) gave product 2 (27.4 g, 56%) as colorless oil: 1H NMR (300 MHz, CDCl3) δ 1.16 (d, J=6.6 Hz, 6H), 2.96-3.04 (m, 1H), 3.87 (s, 3H), 7.47 (d, J=10.5 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07250433B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-df4e111da33945948d792734eb28e3c6 |
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| Source note | uspto-grants-2007_07 |
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