HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 889026Generated: November 1, 2026
Ethanol → 1-(4-Isopropyl-phenyl)-5-oxo-pyrrolidine-3-carboxylic acid ethyl ester
https://huagongshe.com/reaction/889026
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 1-(4-Isopropylphenyl)-5-oxopyrrolidine-3-carboxylic acid | HCID 3151003 | — |
| Product | 1-(4-Isopropyl-phenyl)-5-oxo-pyrrolidine-3-carboxylic acid ethyl ester | HCID 50873721 | 100% |
Reaction Steps
A mixture of 1-(4-isopropyl-phenyl)-5-oxo-pyrrolidine-3-carboxylic acid obtained in step 1 (0.6 g, 2.42 mmol), thionyl chloride (0.35 g, 2.90 mmol), and ethanol (10 ml) was heated at 55-60° C. for 2 hours. The mixture was cooled and solvent was removed. The residue was dissolved in ethyl acetate (20 ml). The organic layer was washed with saturated NaHCO3 and saturated brine solution (20 ml). The organic layer was dried over Na2SO4 and evaporated to obtain 1-(4-isopropyl-phenyl)-5-oxo-pyrrolidine-3-carboxylic acid ethyl ester as yellow oil (0.7 g, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08252797B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-549c075cf75a45dc8520e3b5311bd618 |
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| Source note | uspto-grants-2012_08 |
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