HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → 3-(2-Cyclopentyl-2-phenyl-2-hydroxyacetoxy)-1-(ethoxycarbonylmethyl)-1-methylpyrrolidinium bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | N-Methyl-3-pyrrolidinyl Cyclopentylmandelate | HCID 25727 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-(2-Cyclopentyl-2-phenyl-2-hydroxyacetoxy)-1-(ethoxycarbonylmethyl)-1-methylpyrrolidinium bromide | HCID 16722848 | — |
Reaction Steps
To compound 4 (0.369 g, 122 mmol) in 10 ml of dry acetonitrile, ethyl bromoacetate (0.377 g, 2.25 mmol) was added at room temperature. The mixture was stirred for 2 h. Evaporation of acetonitrile gave a crude product. The crude product was dissolved in a small volume of ethylene chloride and then poured into 50 ml of dry ethyl ether to precipitate. This procedure was repeated three times to obtain Compound (b) as pure product (0.45 g, 79%). White powder, m.p.: 192-194° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08628759B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-1ecce122ac4f4f2da0dc7e3b8edf058e |
| Source note | uspto-grants-2014_01 |