HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Dioxide → HCID 23452583, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2-(alpha-Ethoxycarbonyl-4-chlorobenzylidene)-1-isopropylpyrrolidine | HCID 53781790 | — |
| Catalyst | HCID 178506450 | HCID 178506450 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 23452583 | HCID 23452583 | — |
Reaction Steps
Boil 40.6 g of 2-(α-ethoxycarbonyl-4-chlorobenzylidene)-1-isopropylpyrrolidine and 115 ml of conc. hydrochloric acid under reflux until evolution of carbon dioxide ceases. Alkalize the resulting reaction mixture with 250 ml of 6 N sodium hydroxide solution before extracting with 400 ml of diethyl ether, dry the ether phase over sodium sulfate and concentrate it. Dissolve thus-obtained residue in 250 ml of ethanol, and hydrogenate the resulting solution with platinum/hydrogen. Then filter off the catalyst and distil off the solvent before distilling the product under a high vacuum to obtain a yield [21.8 g (70% of theory)] of title compound and having a b.p. of 75° at 7·10-3 mm of Hg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04279918 |
| Source dataset | uspto-grants-1981_07 |
| ORD ID | ord-d9d447cb75c84b98ac4f0efdbdcbaeb8 |
| Source note | uspto-grants-1981_07 |