Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Propionic Acid | HCID 1032 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | HCID 57429412 | HCID 57429412 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | HCID 57429416 | HCID 57429416 | 800% |
Reaction Steps
A solution of 3-(3-isopropylcyclohexyl)butanal (6 g, 30.5 mmol) in isopropanol (3.5 mL) followed by formaldehyde (37% wt in water, 30.5 mmol, 1 eq) was charged into a 50 mL three-necked round-bottom flask equipped with a reflux condenser and a mechanical stirrer. Propionic acid (228 L, 3.0 mmol, 0.1 eq) and pyrrolidine (255 L, 3.0 mmol, 0.1 eq) were added at ambient temperature. The reaction mixture was then stirred at 45° C. for 3 h. The crude mixture was cooled to ambient temperature dissolved in MTBE (100 mL) and washed with saturated aqueous NaHCO3 (100 mL), brine (100 mL), dried over magnesium sulphate and concentrated. The crude product was chromatographed on a silica gel column with 3% EtOAc in hexane as elution agent giving 3-(3-isopropylcyclohexyl)-2-methylenebutanal (5 g, gc purity>99%; yield 78%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08709994B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-cd542ebc7880482095f1debb09c64df4 |
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| Source note | uspto-grants-2014_04 |
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