HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 15085902, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 15085897 | HCID 15085897 | — |
| Reactant | HCID 15085901 | HCID 15085901 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 15085902 | HCID 15085902 | — |
| Product | HCID 15085903 | HCID 15085903 | — |
Reaction Steps
4,4-Difluoro-17β-(cyclopropyloxy)androst-5-en-3β-ol is treated with acetic anhydride and pyridine. The mixture is poured into water and extracted with ethyl acetate. The ethyl acetate layer is separated and dried and the solvent is evaporated to leave as a residue, 3β-acetyloxy-4,4-difluoro-17β-(cyclopropyloxy)androst-5-ene. 3β-(Cyclopentanepropionyloxy)-4,4-difluoro-17β-(cyclopropyloxy)androst-5-ene and 3β-(benzenepropionyloxy)-4,4-difluoro-17β-(cyclopropyloxy)androst-5-ene are obtained in a similar way using the appropriate acid chlorides.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04966897 |
| Source dataset | uspto-grants-1990_10 |
| ORD ID | ord-a81193e0660c44fc8e0a23bacc2bfbc7 |
| Source note | uspto-grants-1990_10 |