Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Propionic Acid | HCID 1032 | — |
| Reactant | 1,3-Pentadiene, 2-methyl- | HCID 14238 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | Crotonaldehyde | HCID 447466 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 44542715 | HCID 44542715 | 50% |
Reaction Steps
To a mixture of crotonic aldehyde (165.2 g, 2.36 mol), 2-methyl-penta-1,3-diene (361.6 g, 4.41 mol) and formalin (37% in water (200 g, 2.46 mol) was added a mixture of pyrrolidine (16.0 g, 0.22 mol) and propionic acid (17.0 g, 0.23 mol). The mixture was placed in an autoclave and heated to 60-100° C. for 8 h. The reaction mixture was cooled to room temperature, diluted with sat. NaHCO3 and extracted 3 times with MTBE (200 ml). The combined org. layers were washed with brine (200 ml), dried (MgSO4) and evaporated in vacuo. The residue was purified by distillation to give 2,4-dimethyl-1-vinylcyclohex-3-enecarbaldehyde (50% yield). Boiling point: 50-53° C./0.15 mbar.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08691746B2 |
|---|
| Source dataset | uspto-grants-2014_04 |
|---|
| ORD ID | ord-a65998b2c4db406ab5b0fa20c7e6bdd5 |
|---|
| Source note | uspto-grants-2014_04 |
|---|