HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Ethyl 1-benzyl-1,4,5,6-tetrahydrocyclopenta[b]pyrrole-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl bromopyruvate | HCID 66144 | — |
| Reactant | N-Benzylcyclopentanimine | HCID 12350908 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 1-benzyl-1,4,5,6-tetrahydrocyclopenta[b]pyrrole-2-carboxylate | HCID 13592288 | — |
Reaction Steps
Add dropwise 3.9 gm of ethyl bromopyruvate in 50 ml of ethanol to a flask containing 3.46 gm of benzyliminocyclopentane and 2.0 g of triethylamine in 50 ml of ethanol at 0° C., stir for 2 hours, then heat to reflux for 2 hours. Concentrate the reaction mixture and partition between 1N HCl and ether. Dry the ether extract over magnesium sulfate, filter, ooncentrate under high vacuum to obtain a brown oil and distill in a kugelrohr at 190°-210°/0.1 mm to obtain the title compound of Part A as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04831157 |
| Source dataset | uspto-grants-1989_05 |
| ORD ID | ord-ebb01ef61b3a41e99c36613a9f7b9272 |
| Source note | uspto-grants-1989_05 |