HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 13135602, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 13135599 | HCID 13135599 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 13135602 | HCID 13135602 | 76.2% |
Reaction Steps
In 4 ml of methylene chloride was dissolved 223 mg of 11β,21-dihydroxy-17α-methoxyacetoxy-6α-methyl-1,4-pregnadiene-3,20-dione obtained according to the method as described in Example 32. To this solution were added 404 mg of triethylamine and 204 mg of acetic anhydride, and the mixture was stirred for 5 hours at room temperature. The reaction mixture was then treated in the same manner as described in Example 7 whereby 186 mg (yield: 76.2%) of the title compound was obtained as colorless needle crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04567172 |
| Source dataset | uspto-grants-1986_01 |
| ORD ID | ord-5f7dcfbaba8540f1b022690156ba76db |
| Source note | uspto-grants-1986_01 |