HuagongsheHuagongshe Chemistry Print Report · For research reference only
(1beta,2beta)-17-(Acetyloxy)-1,2-dihydro-3'H-cyclopropa[1,2]pregna-1,4,6-triene-3,20-dione → 17alpha-Acetoxy-1alpha,2alpha-methylene-4-pregnene-3,20-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (1beta,2beta)-17-(Acetyloxy)-1,2-dihydro-3'H-cyclopropa[1,2]pregna-1,4,6-triene-3,20-dione | HCID 13519086 | — |
| Catalyst | Calcium Palladium Carbonate | HCID 12000666 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 17alpha-Acetoxy-1alpha,2alpha-methylene-4-pregnene-3,20-dione | HCID 13519088 | — |
Reaction Steps
A solution of 60.0 g of 17α-acetoxy-1α,2α-methylene-4,6-pregnadiene-3,20-dione [R. Wiechert et al., Chem. Ber. 93: 1710 (1960)] in 1.25 1 of dimethylformamide is combined with 6.3 g of 10% Pd/CaCO3 and then hydrogenated. After a hydrogen absorption of 5.1 1, the catalyst is filtered off and the reaction solution stirred into ice water. The precipitate is suctioned off, worked up as usual, and the crude product is purified on 1.5 kg of silica gel with a pentane-acetone gradient (0-30% acetone). Yield: 34.3 g of 17α-acetoxy-1α,2α-methylene-4-pregnene-3,20-dione, mp 268°-270° C. [α]D =+215°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04670427 |
| Source dataset | uspto-grants-1987_06 |
| ORD ID | ord-2f07803788444daf870a82e1fbd330b3 |
| Source note | uspto-grants-1987_06 |