HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → (3S,4S)-3-(tert-Butoxycarbonyl)amino-4-vinylpyrrolidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | (3S,4S)-1-Benzyloxycarbonyl-3-(tert-butoxycarbonyl)amino-4-vinylpyrrolidine | HCID 59665269 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (3S,4S)-3-(tert-Butoxycarbonyl)amino-4-vinylpyrrolidine | HCID 22880744 | — |
Reaction Steps
A solution of (3S,4S)-1-benzyloxycarbonyl-3-(tert-butoxycarbonyl)amino-4-vinylpyrrolidine (275 mg, 0.794 mmol) in tetrahydrofuran (5 mL) and sodium (300 mg, 13.0 mmol) were sequentially added to liquid ammonia (80 mL) at −78° C., and the mixture was stirred at the same temperature for 0.5 hours. The solvent was removed, followed by dilution with chloroform (80 mL). The resultant mixture was washed sequentially by 1 mol/L sodium hydroxide (30 mL) and saturated brine (100 mL), dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure, to thereby yield the title compound as a colorless oily substance (168 mg, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07977327B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-9930d39bb8a74bed8109d735663d82fd |
| Source note | uspto-grants-2011_07 |