HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,2,2-Trichloroethyl chloroformate → Ethyl 4-(3,4-dichlorophenyl)pyrrolidine-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,2,2-Trichloroethyl chloroformate | HCID 87063 | — |
| Reactant | Ethyl 1-benzyl-4-(3,4-dichlorophenyl)pyrrolidine-3-carboxylate | HCID 67131665 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Ethyl 4-(3,4-dichlorophenyl)pyrrolidine-3-carboxylate | HCID 67327572 | 97.1% |
Reaction Steps
To a solution of (3SR,4RS)-1-benzyl-4-(3,4-dichloro-phenyl)-pyrrolidine-3-carboxylic acid ethyl ester (2.50 g, 6.61 mmol) in CH3CN (55 mL) was added 2,2,2-trichloroethyl chloroformate (1.34 mL, 9.91 mmol) and stirring was continued for 4 hours at RT. Volatiles were removed under vacuo, and the residue was dissolved in AcOH (25 mL). Then Zn dust (1.20 g) was added portion wise. After three hours at RT the reaction mixture was filtered on celite, the solvent removed under vacuo followed by an extraction with EtOAc/aq. NaHCO3 (basic pH). The organic phases were dried on Na2SO4 and column chromatography (SiO2, CH2Cl2/MeOH 9:1) yielded 1.85 g (97%) of the title compound as a light yellow oil. ES-MS m/e: 288.1 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08318759B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-9b06aae80d294dae9aafc3afd2698dc5 |
| Source note | uspto-grants-2012_11 |