Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | HCID 57255885 | HCID 57255885 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | HCID 13189987 | HCID 13189987 | 47.2% |
Reaction Steps
149 g of formic acid were added dropwise to 45.8 g of pyrrolidine, while cooling with ice. 181 g of 3-(2,4-dichlorophenyl)-2-methyl-2-propen-1-ylpropionaldehyde were then added, after which the mixture was heated at 100° C. for 12 hours and then evaporated down under reduced pressure. The residue was made alkaline with 25% strength NaOH and extracted with ether, and the organic phase was dried over KOH and evaporated down. Distillation of the residue gave 95 g of (X) of boiling point 130°-138° C./0.1 mbar.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04472412 |
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| Source dataset | uspto-grants-1984_09 |
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| ORD ID | ord-d92ea961c8484b59bce719f353d61f7f |
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| Source note | uspto-grants-1984_09 |
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