HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen chloride-ethyl acetate → (R)-5-(3,4,5-trifluorophenyl)-3,4-dihydro-2H-pyrrole-2-carboxylic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen chloride-ethyl acetate | HCID 21866389 | — |
| Reactant | ethyl(R)-2-tert-butoxycarbonylamino-5-oxo-5-(3,4,5-trifluorophenyl)pentanoate | HCID 67372607 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (R)-5-(3,4,5-trifluorophenyl)-3,4-dihydro-2H-pyrrole-2-carboxylic acid ethyl ester | HCID 67372567 | 80.2% |
Reaction Steps
To a solution of (R)-2-t-butoxycarbonylamino-5-oxo-5-(3,4,5-trifluorophenyl)valeric acid ethyl ester (22.2 g) in ethyl acetate (30 mL) was added 4 N hydrochloric acid/ethyl acetate (163 mL), and the resultant solution was stirred at room temperature for 3 hours. Solvent was removed by distillation under reduced pressure, and the resulting residue was diluted with ethyl acetate and sodium bicarbonate water. The organic layer was partitioned, washed with brine, and then dried over anhydrous magnesium sulfate. Solvent was removed by distillation under reduced pressure, to thereby obtain the titled compound (12.4 g). The physical properties of this crude product were as follows.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07737141B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-295b411d2e014bcf9b491514f041b68b |
| Source note | uspto-grants-2010_06 |