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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 746156Generated: October 25, 2026

Pivalic anhydride → HCID 13423612, compound

https://huagongshe.com/reaction/746156

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPivalic anhydrideHCID 15234—
ReactantSodium BicarbonateHCID 516892—
Reactant15alpha-Hydroxy-4,9-estradiene-3,17-dioneHCID 13423608—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventTolueneHCID 1140—
ProductHCID 13423612HCID 1342361279%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04603013
Source datasetuspto-grants-1986_07
ORD IDord-47f6b0d8c54840228178dcea94124f2a
Source noteuspto-grants-1986_07