HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 889038Generated: November 1, 2026
Methylparaben → 4-[1-(4-Fluorophenyl)-5-oxo-pyrrolidin-3-ylmethoxy]-benzoic acid methyl ester
https://huagongshe.com/reaction/889038
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methylparaben | HCID 7456 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl azodicarboxylate | HCID 5363146 | — |
| Reactant | 1-(4-Fluorophenyl)-4-(hydroxymethyl)pyrrolidin-2-one | HCID 10465677 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-[1-(4-Fluorophenyl)-5-oxo-pyrrolidin-3-ylmethoxy]-benzoic acid methyl ester | HCID 11724977 | 73.1% |
Reaction Steps
4-Hydroxybenzoic acid methyl ester (0.20 g, 1.314 mmol), 1-(4-fluoro-phenyl)-4-hydroxymethyl-pyrrolidin-2-one (0.33 g, 1.577 mmol), Ph3P (0.345 g, 1.314 mmol) and triethyl amine (0.20 ml, 1.577 mmol) were mixed under argon atmosphere followed by the addition of the dry toluene (10 mL). The reaction mixture was cooled to 0° C. followed by addition of DIAD (0.3 mL, 0.788 mmol) drop wise. The reaction mixture was allowed to warm to room temperature and heated at 80° C. for 24 h. The reaction was quenched with 5% HCl (10 mL), extracted with DCM. The organic layer was dried over Na2SO4 and concentrated to afford the crude product which was purified by flash column chromatography to obtain 4-[1-(4-fluorophenyl)-5-oxo-pyrrolidin-3-ylmethoxy]-benzoic acid methyl ester (0.33 g, 73%) as a white solid.
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-e188843eb730415bb8a70d76db37aad3 |
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| Source note | uspto-grants-2012_08 |
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