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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 962627Generated: October 26, 2026

Hydrochloric Acid → HCID 67617838, compound

https://huagongshe.com/reaction/962627

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
ReactantDiethyl ((2-chlorophenyl)methyl)phosphonateHCID 12520073—
ReactantHCID 54231630HCID 54231630—
SolventDimethylformamideHCID 6228—
SolventPropan-2-one--dichloromethane (1/1)HCID 21584124—
ProductHCID 67617838HCID 67617838—

Reaction Conditions

Temperature70 °C

Reaction Steps

Sodium hydride (60%, 26 mg, 0.66 mmole) was added to a solution of 101 mg. (0.33 mol) of 17-keto-4-methyl-5α-androstan-3-one (F) and 173 mg (0.66 mol) of diethyl 2-chlorobenzylphosphonate in 1.0 ml of dry DMF at room temperature. The mixture was heated at 70° C. in a nitrogen atmosphere with stirring for 110 minutes, cooled, poured into 0.5N HCl (20 ml) and extracted with methylene chloride (3×). The organic phases were combined, washed with water (3×), saturated NaCl solution and dried over magnesium sulfate. The organic phase was concentrated under reduced pressure to yield a tan, gummy solid. Flash chromatography of the crude solid was conducted on a silica gel 60×20 mm column, and eluted with 4:1 methylene chloride/acetone in 6 ml. fractions. Fractions 18-24 contained the product which were combined and evaporated to yield a white solid, mp 205°-208° C., yielding one spot on silica gel TLC using 4:1 methylene chloride/acetone. The proton NMR confirmed the assigned structure for 39.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05760045
Source datasetuspto-grants-1998_06
ORD IDord-29203157d64b4629aaf39fb9ff734350
Source noteuspto-grants-1998_06