HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → (S)-1-[4-[3-(Acetyloxy)-1-pyrrolidinyl]-2-butynyl]-2-pyrrolidinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | 1-(Prop-2-yn-1-yl)pyrrolidin-2-one | HCID 12464313 | — |
| Reactant | acetic acid (S)-pyrrolidin-3-yl ester | HCID 15046661 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | (S)-1-[4-[3-(Acetyloxy)-1-pyrrolidinyl]-2-butynyl]-2-pyrrolidinone | HCID 15046674 | 47.9% |
Reaction Steps
A mixture of 500 mg of (S)-3-acetoxypyrrolidine, 530 mg of N-propargyl-2-pyrrolidinone, 150 mg of paraformaldehyde and 50 mg of cupric chloride in 10 ml of dioxane was stirred at reflux under argon for 4 hours. The dioxane was evaporated, the residue was treated with 5 ml of 1N hydrochloric acid and extracted twice with ether. The aqueous acid was basified with 1 g of sodium bicarbonate and extracted twice with dichloromethane. The extracts were combined, dried, filtered and concentrated in vacuo to an oil. This oil was purified by chromatography (alumina), giving 490 mg of the desired product as a yellow oil, [α]D26 =-3° (c, 1.02, methanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04937235 |
| Source dataset | uspto-grants-1990_06 |
| ORD ID | ord-53b2e45541cf46e1967bdf520c71b437 |
| Source note | uspto-grants-1990_06 |