HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → (3beta,20S)-3-[(1-ethoxyethyl)oxy]pregn-5-en-20-ol acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | (3beta,20S)-3-[(1-ethoxyethyl)oxy]pregn-5-en-20-ol | HCID 54499381 | — |
| Solvent | Water | HCID 962 | — |
| Product | (3beta,20S)-3-[(1-ethoxyethyl)oxy]pregn-5-en-20-ol acetate | HCID 57200658 | — |
Reaction Steps
iii)—A solution of (3β,20S)-3-[(1-ethoxyethyl)oxy]pregn-5-en-20-ol (56.9 g) in a mixture of dry pyridine (144 ml) and acetic anhydride (72.4 ml) was stirred at room temperature for 18 h. Water (482 ml) was added and stirring was continued for another 1 h. The product was extracted into ethyl acetate; the combined organic phases were washed with a saturated aqueous solution of sodium hydrogen carbonate and with brine, dried over sodium sulfate, and concentrated under reduced pressure to give (3β,20S)-3-[(1-ethoxyethyl)oxy]pregn-5-en-20-ol acetate (compound 4; 66.1 g) which was used in the following step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06262282B1 |
| Source dataset | uspto-grants-2001_07 |
| ORD ID | ord-055ad6fdf43a4861955256da6e0d645c |
| Source note | uspto-grants-2001_07 |