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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 27333Generated: October 29, 2026

Pyridine → 17beta-Tetrahydropyranyloxy-5alpha-androstan-4-one

https://huagongshe.com/reaction/27333

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDichloromethaneHCID 6344—
Reactant17beta-Tetrahydropyranyloxy-4beta-hydroxy-5alpha-androstaneHCID 15341896—
Catalystchromium (VI) trioxideHCID 10219390—
SolventWaterHCID 962—
Product17beta-Tetrahydropyranyloxy-5alpha-androstan-4-oneHCID 15341897—

Reaction Steps

To 0.42 ml. of dry pyridine and 6.3 ml. of dry dichloromethane was slowly added 0.264 g. of chromium trioxide and the mixture was stirred for 15 min. at room temperature. To the mixture was added a solution of 175 mg. of the product of Step D in 0.7 ml. of dichloromethane and the resulting mixture was stirred for 20 min. at room temperature. The mixture was diluted with water, extracted with ethyl ether, and washed with 2.5 N sodium hydroxide, water, and brine. The mixture was then dried and evaporated to a clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04220775
Source datasetuspto-grants-1980_09
ORD IDord-7a6bd310f23044b3a8a42f553dc70e79
Source noteuspto-grants-1980_09