HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 621624Generated: November 1, 2026
Potassium sodium tartarate → 3,17-Bis(ethylenedioxy)-16-fluoro-5-hydroxy-1beta-methyl-7-methylenandrostane
https://huagongshe.com/reaction/621624
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium sodium tartarate | HCID 9855836 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | 3,17-Bis(ethylenedioxy)-5,6alpha-epoxy-16alpha-fluoro-1beta-methyl-7-methylenandrostane | HCID 86742955 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3,17-Bis(ethylenedioxy)-16-fluoro-5-hydroxy-1beta-methyl-7-methylenandrostane | HCID 86742956 | — |
Reaction Steps
To a solution of lithium aluminium hydride (38 mg) in diethylether (10 ml) is added gradually a solution of 3,17-bis(ethylenedioxy)-5,6α-epoxy-16α-fluoro-1β-methyl-7-methylenandrostane (431 mg) in tetrahydrofuran (10 ml). The resulting mixture is stirred at 20°-25° C. for a period of about 18 hrs after which an aqueous solution of potassium sodium tartrate is added. The mixture is filtered and concentrated to a small volume under reduced pressure. The concentrate is taken up in diethyl ether and washed well with water. The ether solution is dried over magnesium sulfate, filtered and the ether removed under vacuum to yield crude 3,17-bis(ethylenedioxy)-16-fluoro-5-hydroxy-1β-methyl-7-methylenandrostane. This intermediate is dissolved in a 2:1 mixture of acetic acid and water (5 ml) and the solution heated for 6 hrs at 40°-50° C. Then water is added and the product extracted with ethyl acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04824830 |
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| Source dataset | uspto-grants-1989_04 |
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| ORD ID | ord-a153d99df9df4fe4a9bed6f3732bb309 |
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| Source note | uspto-grants-1989_04 |
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