HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 962627Generated: October 26, 2026
Hydrochloric Acid → HCID 67617838, compound
https://huagongshe.com/reaction/962627
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Diethyl ((2-chlorophenyl)methyl)phosphonate | HCID 12520073 | — |
| Reactant | HCID 54231630 | HCID 54231630 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Propan-2-one--dichloromethane (1/1) | HCID 21584124 | — |
| Product | HCID 67617838 | HCID 67617838 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05760045 |
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| Source dataset | uspto-grants-1998_06 |
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| ORD ID | ord-29203157d64b4629aaf39fb9ff734350 |
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| Source note | uspto-grants-1998_06 |
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