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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1837126Generated: November 3, 2026

4-Nitrophenol → HCID 21310344, compound

https://huagongshe.com/reaction/1837126

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-NitrophenolHCID 980—
ReactantSodium IodideHCID 5238—
ReactantTriethylamineHCID 8471—
ReactantHCID 86719952HCID 86719952—
SolventDimethylformamideHCID 6228—
SolventAcetonitrileHCID 6342—
ProductHCID 21310344HCID 2131034451.3%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of 21-bromo-3α-hydroxy-3β-methyl-5α-pregnan-20-one (250 mg, 0.61 mmol), 4-nitrophenol (127 mg, 0.912 mmol), triethylamine (127 μL, 0.912 mmol), and a small amount of sodium iodide in 2:1 acetonitrile:DMF was stirred with heating to ˜60° C. for 6 hours. The mixture was partitioned between EtOAc and 1:1 water:sat. aq. sodium bicarbonate. The organic layer was washed with 2N HCl, water and sat. aq. NaCl, dried with Na2SO4 and concentrated in vacuo. The crude residue was subjected to flash column chromatography. Elution with 20% acetone in hexane yielded 3α-hydroxy-3β-methyl-21-(4′-nitrophenoxy)-5α-pregnan-20-one (147 mg) as a solid; mp 169-172° C.; TLC Rf (hexane:acetone 4:1)=0.35.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06780853B1
Source datasetuspto-grants-2004_08
ORD IDord-a0e7bad81bce4181b9ed3f0ba0d17fa4
Source noteuspto-grants-2004_08