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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1762290Generated: October 31, 2026

Triethylamine → Ethyl 1-benzyl-1,4,5,6-tetrahydrocyclopenta[b]pyrrole-2-carboxylate

https://huagongshe.com/reaction/1762290

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl bromopyruvateHCID 66144—
ReactantN-BenzylcyclopentanimineHCID 12350908—
SolventEthanolHCID 702—
ProductEthyl 1-benzyl-1,4,5,6-tetrahydrocyclopenta[b]pyrrole-2-carboxylateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04831157
Source datasetuspto-grants-1989_05
ORD IDord-ebb01ef61b3a41e99c36613a9f7b9272
Source noteuspto-grants-1989_05