HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 21-Acetoxy-3,3-ethylenedioxy-20-nitropregna-5,16-dien-9alpha-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 3,3-Ethylenedioxy-20-nitropregna-5,16-diene-9alpha,21-diol | HCID 54277511 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 21-Acetoxy-3,3-ethylenedioxy-20-nitropregna-5,16-dien-9alpha-ol | HCID 57121005 | — |
Reaction Steps
Acetic anhydride (1.5 ml) was added to a stirred suspension of 3,3-ethylenedioxy-20-nitropregna-5,16-diene-9α,21-diol (1.00 g of diastereomer II, prepared according to example 2), and 4-dimethylaminopyridine (100 mg) in methylene chloride (10 ml) to give a clear solution. The reaction mixture was stirred for an additional 30 minutes and concentrated under reduced pressure. The residue was dissolved in methylene chloride and filtered over a silica gel column. The filtrate was evaporated under reduced pressure to afford a white solid which was dried under reduced pressure at 50° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05194602 |
| Source dataset | uspto-grants-1993_03 |
| ORD ID | ord-bfd665e02d7842369a83420e9194bc70 |
| Source note | uspto-grants-1993_03 |