Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Malonic Acid | HCID 867 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Piperidinium acetate | HCID 3014295 | — |
| Reactant | 17522-24-6 | HCID 11040651 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Catalyst | Piperidine | HCID 8082 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 86644217 | HCID 86644217 | 44% |
Reaction Steps
At room temp., a piperidinium acetate solution, freshly prepared by mixing piperidine (35.0 μL, 0.354 mmol) and acetic acid (19.0 μL, 0.332 mmol) in dimethyl sulfoxide (1.00 mL), was injected into a stirred solution of the prepared hept-5-ynal (1.50 g, 13.6 mmol) and malonic acid (2.83 g, 27.2 mmol) in dimethyl sulfoxide (50 mL). After refluxing the reaction mixture for 4 h, water (10 mL) and ether (20 mL) were added at room temp., and the layers were separated. The aqueous layer was extracted with ether (3×25 mL), and the combined organic extracts were washed with water (25 mL), dried (Na2SO4), and concentrated under reduced pressure. Kugelrohr distillation at 149° C./14 mbar furnished (3E)-non-3-en-7-ynoic acid (902 mg, 44%) as colorless crystals (mp 43-45° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08217185B2 |
|---|
| Source dataset | uspto-grants-2012_07 |
|---|
| ORD ID | ord-20e5c06706c24d5aaf37e7af1ab364dc |
|---|
| Source note | uspto-grants-2012_07 |
|---|