HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → (15alpha)-15-(Acetyloxy)androst-4-ene-3,17-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 15alpha-Hydroxyandrost-4-ene-3,17-dione | HCID 11652383 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (15alpha)-15-(Acetyloxy)androst-4-ene-3,17-dione | HCID 57023990 | — |
Reaction Steps
168 g of 15α-hydroxy-4-androstene-3,17-dione in 250 ml of pyridine and 125 ml of acetic anhydride are heated on a steam bath. After 90 minutes, the reaction mixture is stirred into ice/water. The thus-precipitated product is suctioned off, taken up in methylene chloride, washed with water, and dried over sodium sulfate. After recrystallization from ethyl acetate, 120 g of 15α-acetoxy-4-androstene-3,17-dione is obtained, mp 145° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05389624 |
| Source dataset | uspto-grants-1995_02 |
| ORD ID | ord-f75258ca317d4ca98f55479aa6368edc |
| Source note | uspto-grants-1995_02 |