HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 57242274, compound → HCID 22859256, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 57242274 | HCID 57242274 | — |
| Catalyst | Hydrochloric Acid | HCID 313 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 22859256 | HCID 22859256 | 74.7% |
Reaction Steps
In methanol (50 ml) was suspended (2S, 3S)-2-acetoxy-3-[[N-valproyl-(L)-valyl]amino]tetrahydrofuran (0.55 g) followed by addition of concentrated hydrochloric acid (5 drops) and the mixture was stirred at room temperature for 1 hour. The reaction mixture was then concentrated under reduced pressure to obtain (2S,3S)-2-methoxy-3-[[N-valproyl-(L)-valyl]amino]tetrahydrofuran (chemical structure below) (0.38 g, 72%). As recrystallized from ethyl acetate, colorless crystals, m.p. 150°-156° C., optical rotation [α]D+ 18.5° (c=0.50, CHCl3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05496834 |
| Source dataset | uspto-grants-1996_03 |
| ORD ID | ord-8d375edf9ebb4e4c821c0d563805560b |
| Source note | uspto-grants-1996_03 |