HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 22790410, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 13beta-Methyl-3-hydroxygona-1,3,5(10),8,14-pentaen-17one | HCID 27234258 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 22790410 | HCID 22790410 | — |
Reaction Steps
Mix 13β-methyl-3-hydroxygona-1,3,5(10),8,14-pentaen-17one with pyridine (3 cc) and acetic anhydride (1 cc) and keep at room temperature for 4 hours. Add ethanol (1 cc) and remove low-boiling material under reduced pressure (0.1 mm) to leave a red gum which crystallizes from a mixture of ethyl acetate and light petroleum. Recrystallize from methanol to obtain crystals of 13β-methyl-3-acetoxygona-1,3,5(10),8,14-pentaen-17-one, melting partially at 161°-166° with resolidification at about 220° and finally melting at 260°-265° (decomp.); infrared absorption peaks at 5.75 μ and 8.27 μ, with absence of an absorption band due to a hydroxy group; ultraviolet absorption peak at 307.5 mμ (ε24,000).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03959322 |
| Source dataset | uspto-grants-1976_05 |
| ORD ID | ord-62ea9487781f41aba8ce5bef8aa43b3e |
| Source note | uspto-grants-1976_05 |