Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 3-chloro-2-methyl-2-pentenal | HCID 583269 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 53851665 | HCID 53851665 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 53904285 | HCID 53904285 | 27.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06063782 |
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| Source dataset | uspto-grants-2000_05 |
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| ORD ID | ord-80bcda634da64577800b11f9703003a1 |
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| Source note | uspto-grants-2000_05 |
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