HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 746156Generated: October 25, 2026
Pivalic anhydride → HCID 13423612, compound
https://huagongshe.com/reaction/746156
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pivalic anhydride | HCID 15234 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 15alpha-Hydroxy-4,9-estradiene-3,17-dione | HCID 13423608 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 13423612 | HCID 13423612 | 79% |
Reaction Steps
A suspension of 19.5 g of 15α-hydroxy-4,9-estradiene-3,17-dione in 300 ml of toluene is mixed, under ice water cooling, successively with 26.5 g of pivalic acid anhydride and 18.6 g of 4-dimethylaminopyridine. Stirring is then performed for 72 hours at room temperature, then the reaction solution is poured into saturated sodium hydrogen carbonate solution, stirred for 30 more minutes at room temperature and extracted with ethyl acetate. The ethyl acetate extracts are washed with saturated ammonium chloride solution and saturated sodium chloride solution, dried with sodium sulfate and concentrated in a water jet vacuum. The crude product, thus obtained, is filtered with aluminum oxide, Merck, neutral, step III, with hexane/ethyl acetate. The main fraction is crystallized from ethyl acetate. 14.4 g (79% of theory) of 4,9,15-estratriene-3,17-dione with a melting point of 182° to 183° C. are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04603013 |
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| Source dataset | uspto-grants-1986_07 |
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| ORD ID | ord-47f6b0d8c54840228178dcea94124f2a |
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| Source note | uspto-grants-1986_07 |
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