HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 362696Generated: October 26, 2026
Trifluoroacetic acid → HCID 54461475, compound
https://huagongshe.com/reaction/362696
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | Diethyl 1-Acetyl-5-hydroxy-3-ethylpyrrolidine-2,2-dicarboxylate | HCID 11289610 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 54461475 | HCID 54461475 | — |
Reaction Steps
To a solution of diethyl 1-acetyl-5-hydroxy-3-ethyl-pyrrolidine-2,2-dicarboxylate (287 g, 0.95 mol) and triethylsilane (228 mL, 1.43 mol) in CH2Cl2 (3 L) under argon was added trifluoroacetic acid (735 mL, 9.53 mol) dropwise with stirring while maintaining the internal temperature at 25° C. by means of an ice bath. After stirring for 3 h at 23° C., the solution was concentrated in vacuo, the residue diluted with CH2Cl2 (1.5 L), then treated with H2O (1 L) and solid Na2CO3 with vigorous stirring until the solution was basic. The organic layer was separated, dried (Na2SO4), filtered, then concentrated to give the title compound as a yellow oil which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05869682 |
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| Source dataset | uspto-grants-1999_02 |
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| ORD ID | ord-5b9e5a9db4244b4bbc465c32f98ba77f |
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| Source note | uspto-grants-1999_02 |
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