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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium sodium tartarateHCID 9855836—
ReactantAluminium lithium hydrideHCID 21226445—
Reactant3,17-Bis(ethylenedioxy)-5,6alpha-epoxy-16alpha-fluoro-1beta-methyl-7-methylenandrostaneHCID 86742955—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product3,17-Bis(ethylenedioxy)-16-fluoro-5-hydroxy-1beta-methyl-7-methylenandrostaneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04824830
Source datasetuspto-grants-1989_04
ORD IDord-a153d99df9df4fe4a9bed6f3732bb309
Source noteuspto-grants-1989_04