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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 27332Generated: October 30, 2026

Hydrogen Peroxide → 17beta-Tetrahydropyranyloxy-4beta-hydroxy-5alpha-androstane

https://huagongshe.com/reaction/27332

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantBoraneHCID 6331—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 15341895HCID 15341895—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product17beta-Tetrahydropyranyloxy-4beta-hydroxy-5alpha-androstaneHCID 15341896—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cooled solution (0° C.) of 5 ml. of 1 M borane in tetrahydrofuran in 2.7 ml. of dry tetrahydrofuran was added 500 mg. (1.4 millimole) of the product of Step C. in 2.0 ml. of dry tetrahydrofuran. The clear solution was stirred for 1 hr. at room temperature and then cooled to 0° C. and treated with 5 ml. of 2.5 N sodium hydroxide followed by 4 ml. of 30% hydrogen peroxide. The solution was stirred for 1 hr. at room temperature, diluted with water and extracted with ethyl ether, washed with water, brine, dried and evaporated to an oily crystalline material. The product was washed with cold methanol and pumped dry to give 175 mg. of final product having a m.p. of 167°-170° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04220775
Source datasetuspto-grants-1980_09
ORD IDord-f7b4b13f31f1474b91baa4a400875309
Source noteuspto-grants-1980_09