HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828068Generated: October 30, 2026
Trifluoroacetic acid → Oxo-[2-(2-phenethyl-4-phenyl-butyryl)-pyrrolidin-1-yl]-acetic acid methyl ester
https://huagongshe.com/reaction/1828068
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(2-Phenethyl-4-phenyl-butyryl)-pyrrolidine-1-carboxylic acid tert-butyl ester | HCID 21027771 | — |
| Reactant | Chlorooxoacetate | HCID 21988599 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Oxo-[2-(2-phenethyl-4-phenyl-butyryl)-pyrrolidin-1-yl]-acetic acid methyl ester | HCID 21027767 | 98.2% |
Reaction Steps
To a solution of 0.18 g (0.40 mmol) of 11a in CH2Cl2 (3 mL) was added dropwise 10 mL (8.77 mmol) of trifluoroacetic acid, and the mixture was allowed to stir for 2 hours. The solution was diluted with CH2Cl2 (10 mL) and cooled to 0° C. followed by dropwise addition of 0.7 g (10.00 mmol) of triethylamine. After 5 minutes, to the solution was added dropwise 0.06 g (0.5 mmol) of chlorooxoacetate, and the mixture was stirred for 2 hours. The solution was quenched with H2O and extracted with CH2Cl2 (2×200 mL). The organic phase was dried (MgSO4) and evaporated to a clear oil which was subject to column chromatography (EtOAc/Hexanes, 1:1) to yield 0.16 g (98.2%) of 12a as a clear oil. TLC Rf=0.6 (EtOAc/Hexanes, 1:3)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07056935B2 |
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| Source dataset | uspto-grants-2006_06 |
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| ORD ID | ord-f34f3b4973d94bd0a8a050f976f8fc43 |
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| Source note | uspto-grants-2006_06 |
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