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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1107793Generated: October 30, 2026

Triethylamine → HCID 53904285, compound

https://huagongshe.com/reaction/1107793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAmmonium ChlorideHCID 25517—
Reactant3-chloro-2-methyl-2-pentenalHCID 583269—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 53851665HCID 53851665—
SolventEthanolHCID 702—
ProductHCID 53904285HCID 5390428527.1%

Reaction Steps

3.74 g (0.024 mole) of ethyl N-(2-butenyl)glycinate were added to a solution of 5.0 g (0.038 mole) of 3-chloro-2-methyl-2-pentenal in 10 ml of ethanol with stirring, and subsequently 6 ml (0.043 mole) of triethylamine were added thereto and stirred at room temperature for 7 hours. After the precipitates deposited were filtered off, 5.35 g (0.048 mole) of potassium tert-butoxide were added to the filtrate by portions and the mixture was stirred for 30 minutes. The reaction mixture was poured into about 150 ml of a saturated aqueous solution of ammonium chloride and extracted with ethyl acetate (once with 100 ml and twice with 50 ml). The combined extracts were washed with a saturated aqueous solution of sodium chloride and dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was purified by column chromatography through silica gel using a 3:97 mixture of ethyl acetate and hexane as an eluent to give 1.53 g of ethyl 1-(2-butenyl)-5-ethyl-4-methylpyrrole-2-carboxylate (cis/trans=76/24) as an orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06063782
Source datasetuspto-grants-2000_05
ORD IDord-80bcda634da64577800b11f9703003a1
Source noteuspto-grants-2000_05