HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 9929412, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 57629370 | HCID 57629370 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 9929412 | HCID 9929412 | — |
Reaction Steps
A mixture of crude 17,17-ethylenedioxyandrosta-1.5-dien-3β-ol (4, 1.2 g) in pyridine (10 ml) and acetic anhydride (3 ml) was stirred at room temperature for 16 hours. The reaction mixture was poured into ice-water and the compound was extracted with ether. The organic layer was washed with ice-water several times followed by brine and dried over anhydrous magnesium sulfate. Evaporation of the solvent in vacuo below 35° C. gave 1.0 g of crude solid. Recrystallization from methanol gave 3β-acetoxy-17,17-ethylenedioxyandrosta-1,5-diene (5). Mp. 105-6° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07514420B2 |
| Source dataset | uspto-grants-2009_04 |
| ORD ID | ord-c35149602ede4a0ca33686c35f7191ca |
| Source note | uspto-grants-2009_04 |