HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Dioxide → 8-ethyl-8-azabicyclo[3.2.1]octan-3-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Trisodium citrate | HCID 6224 | — |
| Reactant | Ethylamine | HCID 6341 | — |
| Reactant | Acetonedicarboxylic acid | HCID 68328 | — |
| Reactant | 2,5-Dimethoxytetrahydrofuran | HCID 79098 | — |
| Solvent | Water | HCID 962 | — |
| Product | 8-ethyl-8-azabicyclo[3.2.1]octan-3-one | HCID 272957 | 46% |
Reaction Steps
52 ml of 2,5-dimethoxy-tetrahydrofuran (0.402 moles) are dissolved in 58 ml of water and acidified with 1.2 ml of 37% hydrochloric acid. After 15 minutes, 58 g of acetonedicarboxylic acid (0.397 moles) are added followed by 40.4 g of tribasic sodium citrate bihydrate (0.137 moles) dissolved in 58 ml of water. 18.5 g of ethylamine (0.411 moles) in 35 ml of water are then dripped in. The mixture is left stirring until carbon dioxide ceases to be evolved. It is then saturated with K2CO3 and extracted with ethyl ether. After drying and evaporating the solvent, the crude product is distilled under vacuum. 27.9 g of 8-ethyl-8-azabicyclo-[3.2.1]-octan-3-one are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04411902 |
| Source dataset | uspto-grants-1983_10 |
| ORD ID | ord-d7fc5ef1874843058f1260b1529652ea |
| Source note | uspto-grants-1983_10 |