HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1870894Generated: November 1, 2026
Triethylamine → 1-(4-bromo-3-methylphenyl)pyrrolidin-2-one
https://huagongshe.com/reaction/1870894
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-Bromo-3-methylaniline | HCID 23359 | — |
| Reactant | 4-Chlorobutyryl chloride | HCID 78370 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(4-bromo-3-methylphenyl)pyrrolidin-2-one | HCID 11218998 | 89.8% |
Reaction Steps
A stirred solution of 4-bromo-3-methylaniline (50.3 g, 0.27 mole) and triethylamine (41.1 ml, 0.30 mole) in THE (250 ml) at 0° C. under argon was treated dropwise with 4-chlorobutyryl chloride (33.4 ml, 0.30 mole). The mixture was stirred for 1 hour at 0-5° C., then potassium t-butoxide (82.5 g, 0.74 mole) was added portionwise over 20 minutes, maintaining temperature below 25° C. The reaction mixture was stirred at 25° C. for a further 2.5 hrs, then treated with water (100 ml), followed after 0.25 hrs with 10% aqueous Na2CO3 solution and then extracted with ethyl acetate. The extract was washed with water, 5M HCl acid, then brine, dried (Na2SO4) and concentrated in vacuo to afford the title compound as a pale yellow solid (61.6 g, 89%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06100272 |
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| Source dataset | uspto-grants-2000_08 |
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| ORD ID | ord-355acfbd772e4d3ab98584800100e01f |
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| Source note | uspto-grants-2000_08 |
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