HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → (2R,4S)-1-(tert-butoxycarbonyl)-4-cyano-2-methylpyrrolidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | HCID 22843271 | HCID 22843271 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | (2R,4S)-1-(tert-butoxycarbonyl)-4-cyano-2-methylpyrrolidine | HCID 22843272 | 71.6% |
Reaction Steps
A solution of (2R,4R)-1-(tert-butoxycarbonyl)-4-methanesulfonyloxy-2-methylpyrrolidine (2.3 g) and sodium cyanide (1.37 g) in dimethyl sulfoxide (25 ml) was heated for two and a half hours at 90° C. The reaction mixture was poured into a mixture of water (100 ml) and ethyl acetate (100 ml). The organic layer was separated, washed with brine, and dried over magnesium sulfate. Evaporation of the solvent gave an oil, which was chromatographed on silica gel (100 ml) eluting with a mixture of hexane and ethyl acetate (4:1, V/V) to give (2R,4S)-1-(tert-butoxycarbonyl)-4-cyano-2-methylpyrrolidine (1.24 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05102877 |
| Source dataset | uspto-grants-1992_04 |
| ORD ID | ord-966eb4f04b4543ff9af49453e34365f5 |
| Source note | uspto-grants-1992_04 |