HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 15723360, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 4-(1-Hydroxyundecyl)-2-trimethylsilylfuran | HCID 19885896 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 15723360 | HCID 15723360 | — |
Reaction Steps
A mixture of 4-(1-hydroxyundecyl)-2-trimethylsilylfuran (1.21 g, 3.89 mmol), acetic anhydride (4 ml) and pyridine (6 ml) was stirred under argon at ca. 20° for 14h. After most of the solvent was removed under high vacuum (<40°), the residue was dissolved in ether (40 ml) and washed thoroughly with aqueous copper sulfate and water. Drying (magnesium sulfate) and evaporation gave a brown oil, which was flash chromatographed on silica using 5% ethyl ether/petroleum ether. Fractions with Rf of about 0.3 on evaporation afforded the captioned compound as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05134128 |
| Source dataset | uspto-grants-1992_07 |
| ORD ID | ord-f54219dae3b040bba35494a3f323ba51 |
| Source note | uspto-grants-1992_07 |