Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Undecanoyl chloride | HCID 87287 | — |
| Reactant | Trestolone | HCID 9838899 | — |
| Product | HCID 9955725 | HCID 9955725 | — |
Reaction Steps
A total of 2.23 grams of commercially available undecanoyl chloride were added to a stirred solution of 1.58 grams of (7α,17β)-17-hydroxy-7-methylestr-4-en-3-one at 0-5° C. reaction mixture was allowed to reach room temperature and stirred overnight. Thereafter, ice was added and after stirring for another 2 hours the reaction mixture was poured into ice-water, containing 4 ml of conc. H2SO4, followed by ethyl acetate extraction. The organic layers were washed with water, cold 1 N NaOH solution and brine, dried on sodium sulfate, filtered and evaporated in vacuo. The residue was chromatographed over silica. Elution with heptane-ethylacetate (4:1) and evaporation gave a greasy solid that was collected. Yield 1.42 g, [α]D20=+36° (c=1; dioxane), MS (ESI): 456.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06437158B1 |
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| Source dataset | uspto-grants-2002_08 |
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| ORD ID | ord-2c15027d5fec4dc3b0b5592732699a86 |
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| Source note | uspto-grants-2002_08 |
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