HuagongsheHuagongshe Chemistry Print Report · For research reference only
Malonic Acid → (2E)-3-[(2S)-2-methyltetrahydro-2H-pyran-4-yl]acrylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Malonic Acid | HCID 867 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | (2S)-2-methyltetrahydro-2H-pyran-4-carboxaldehyde | HCID 57936012 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | (2E)-3-[(2S)-2-methyltetrahydro-2H-pyran-4-yl]acrylic acid | HCID 57935998 | — |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
A mixture of (2S)-2-methyltetrahydro-2H-pyran-4-carboxaldehyde (4.0), malonic acid (6.495 g) and piperidine (0.1 ml) in pyridine (10 ml) was heated to 100° C. for 4 hours. The reaction mixture was concentrated and partitioned between ethyl acetate (100 ml) and 1N HCl. The organic layer was dried, evaporated and recrystallised form toluene to give the title compound. Yield 2.48 g. NMR CDCl3 1.2 (m, 4H), 1.5 (m, 1H), 1.7 (m, 2H), 2.45 (m, 1H), 3.5 (m, 2H), 4.05 (m, 1H), 5.8 (d, 1H), 7.0 (dd, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07615555B2 |
| Source dataset | uspto-grants-2009_11 |
| ORD ID | ord-63a828e8647f4fb991274297a980ec5f |
| Source note | uspto-grants-2009_11 |