HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyrrolidine → 3-(1-Pyrrolidinyl)-9-azabicyclo[3,3,1]non-2-ene-9-carboxylic acid ethylester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | Ethyl 3-oxo-9-azabicyclo[3.3.1]nonane-9-carboxylate | HCID 54360990 | — |
| Catalyst | Titanium Tetrachloride | HCID 24193 | — |
| Product | 3-(1-Pyrrolidinyl)-9-azabicyclo[3,3,1]non-2-ene-9-carboxylic acid ethylester | HCID 53882570 | — |
Reaction Steps
At room temperature, under a nitrogen atmosphere and with stirring, a solution of 110 g of titanium tetrachloride in 450 ml of petroleum ether is added dropwise, within 2.5 hours, to a solution of 223 g of 9-azabicyclo-[3,3,1]nonan-3-one-9-carboxylic acid ethyl ester (e) and 300 g of pyrrolidine in 2.5 liters of absolute petroleum ether (b.p. 50° to 70° C.). The mixture is stirred for 24 hours. The light-yellow precipitate formed is filtered, suspended in benzene, suctionfiltered and washed with benzene. The united filtrates are concentrated in a vacuum; the orange-red oil which remains behind is purified through vacuum distillation to obtain 260 g (93.5 percent) of yellow, viscous oil (b.p. 140° C. at 6.7 Pa.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04277472 |
| Source dataset | uspto-grants-1981_07 |
| ORD ID | ord-141b6bfc8f5b48429eeec9999cd8a81a |
| Source note | uspto-grants-1981_07 |