Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 582519Generated: October 31, 2026

p-Toluenesulfonic acid → HCID 69905541, compound

https://huagongshe.com/reaction/582519

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantSulfolaneHCID 31347—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 69904879HCID 69904879—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 69905541HCID 6990554119.1%

Reaction Conditions

Temperature110 °C

Reaction Steps

To a mixture of 2β-isopropoxy-3α-hydroxy-5α-androstan-17-one tosylhydrazone (300 mg), NaBH3CN (144 mg) and p-toluenesulfonic acid (30 mg) was added DMF and sulfolane (1:1, 3 mL) and the mixture obtained was heated to 110° C. for 3 h. Then additional amount of NaBH3CN (144 mg) and p-toluenesulfonic acid (30 mg) was added and it was heated for another hour. Water was then added and the mixture was extracted with EtOAc (2×45 mL). The combined extracts were dried over Na2SO4 and the crude product obtained by removal of the solvent was purified by flash chromatography over silica gel to yield the pure 2β-isopropoxy-3α-hydroxy-5α-androstane (37 mg); TLC Rf (EtOAc:hexane 1:9)=0.17.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05925630
Source datasetuspto-grants-1999_07
ORD IDord-d9281a591d1a4566b7bab6340deddc22
Source noteuspto-grants-1999_07