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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1580210Generated: November 2, 2026

Pyridine → Ethyl 9-ethylenedioxy-15-oxo-prostanoate

https://huagongshe.com/reaction/1580210

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantEthyl 9-ethylenedioxy-15-hydroxy-prostanoateHCID 68124126—
Catalystchromium (VI) trioxideHCID 10219390—
SolventDichloromethaneHCID 6344—
ProductEthyl 9-ethylenedioxy-15-oxo-prostanoateHCID 68123704—

Reaction Steps

A solution of 8.7 g. of dry pyridine in 140 ml. of dry methylene chloride, stirred in a tap water bath is treated with 5.5 g. of dry chromium trioxide. The resulting deep red suspension is stirred at ambient temperature for 15 minutes. A solution of 3.78 g. of ethyl-9-ethylenedioxy-15-hydroxy-prostanoate (Example 55) in 15 ml. of methylene chloride is added, all at once, to the suspension. A black, tarry deposit is formed immediately. After stirring for 15 minutes at ambient temperature, the methylene chloride solution is decanted from the tarry deposit which is triturated with several portions of ether. The combined organic phases are washed with 5% aqueous sodium hydroxide, water, ice-cold 5% aqueous hydrochloric acid, saturated sodium bicarbonate solution, and saturated sodium chloride solution, dried with anhydros magnesium sulfate and taken to dryness to give 3.29 g. (88%) of a viscous oil; λ max 5.78 and 5.86 μ (carbonyl groups).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03932463
Source datasetuspto-grants-1976_01
ORD IDord-3c057f6eee5247c2ae64d21e8339afce
Source noteuspto-grants-1976_01