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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650342Generated: October 28, 2026

Ammonium Chloride → 3-Benzyloxy-7alpha-(5-hydroxypentyl)-15beta-methyl-estra-1,3,5(10)-trien-17-one

https://huagongshe.com/reaction/650342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant3-Benzyloxy-7alpha-(5-hydroxypentyl)-estra-1,3,5(10),15-tetra-en-17-oneHCID 57272166—
ReactantHCID 178418573HCID 178418573—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product3-Benzyloxy-7alpha-(5-hydroxypentyl)-15beta-methyl-estra-1,3,5(10)-trien-17-oneHCID 69963503—

Reaction Conditions

Temperature0 °C

Reaction Steps

5.35 g of copper(I) iodide is added to an ice-cooled solution of 11.9 ml of a 3-molar methylmagnesium bromide solution in 68 mnl of tetrahydrofuran under a nitrogen stream. Then, a solution of 4.26 g of 3-benzyloxy-7α-(5-hydroxypentyl)-estra-1,3,5(10),15-tetraen-17-one (see Example 6b) in 50 ml of tetrahydrofuran is added in drops and stirred for 30 minutes at a bath temperature of 0° C. Then, the excess reagent is decomposed with saturated ammonium chloride solution, diluted with ethyl acetate, washed with ammonium chloride solution and water, dried on sodium sulfate, concentrated by evaporation in a vacuum and chromatographed on silica gel with hexane/acetone. 3.6 g of 3-benzyloxy-7α-(5-hydroxypentyl)-15β-methyl-estra-1,3,5(10)-trien-17-one is obtained as oil. [α]D22 =+66.4°(c=0.515% in chloroform).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06271403B1
Source datasetuspto-grants-2001_08
ORD IDord-7f6ad95d646c4bed8b9def36ca0ce3d0
Source noteuspto-grants-2001_08