HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diiodomethane → 1beta,2beta-Methylene-19-tetrahydropyranyloxy-5-androstene-3beta,17beta-diol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diiodomethane | HCID 6346 | — |
| Reactant | 1,2-Dimethoxyethane | HCID 8071 | — |
| Reactant | 19-Tetrahydropyranyloxy-1,5-androstadiene-3beta,17beta-diol | HCID 22806903 | — |
| Catalyst | Zinc copper couple | HCID 10290809 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1beta,2beta-Methylene-19-tetrahydropyranyloxy-5-androstene-3beta,17beta-diol | HCID 70605094 | — |
Reaction Steps
To a stirred solution of 19-tetrahydropyranyloxy-1,5-androstadiene-3β,17β-diol in a mixture of dry ether and glyme is added zinc-copper couple and methylene iodide. This reaction mixture is refluxed for four hours, cooled to room temperature, diluted with ether and filtered. The ether filtrate is washed with an aqueous sodium chloride solution, washed with water, and dried over anhydrous magnesium sulfate. The ether is removed under reduced pressure and the residue which remains is crystallized from an acetone-hexane solution to yield 1β,2β-methylene-19-tetrahydropyranyloxy-5-androstene-3β,17β-diol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04139617 |
| Source dataset | uspto-grants-1979_02 |
| ORD ID | ord-9e0834e2f38844af8b01ab1d04fa277c |
| Source note | uspto-grants-1979_02 |