HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 13556431, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Selenazofurin | HCID 100665 | — |
| Product | HCID 13556431 | HCID 13556431 | — |
Reaction Steps
A mixture of 2-β-D-ribofuranosylselenazole-4-carboxamide (1.0 g, 3.25 mmol), N,N-dimethylaminopyridine (catalyst, 80 mg) and acetic anhydride (15 ml) was stirred at room temperature for 3 hours. The solvent was evaporated in vacuo and coevaporated with water (10 ml×2) to provide COMPOUND 3 as a white crystalline product which was triturated with water and collected by filtration. The product was recrystallized from water containing a few drops of ethanol to provide white needles: yield 1.2 g (85 percent), mp 117-119 degrees C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04594414 |
| Source dataset | uspto-grants-1986_06 |
| ORD ID | ord-157c1eb09c2a4193814abbfad2622b41 |
| Source note | uspto-grants-1986_06 |