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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 905149Generated: October 30, 2026

HCID 13216544, compound → HCID 178449935, compound

https://huagongshe.com/reaction/905149

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 13216544HCID 13216544—
ReactantHCID 19001768HCID 19001768—
SolventEthanolHCID 702—
SolventSodium AcetateHCID 517045—
ProductHCID 178449935HCID 178449935—

Reaction Conditions

Temperature20 °C

Reaction Steps

10.0 parts by weight of 2-butyryl-4-methoxycarbonyl-5-[tetrahydropyran-4-ylmethyl]-cyclohexane-1,3-dione were dissolved in 150 parts by volume of ethanol, and 2.93 parts by weight of ethoxyammonium chloride and 2.71 parts by weight of anhydrous sodium acetate were added. The mixture was stirred at 20° C. for 20 hours, poured into ice-water and extracted with methylene chloride. The organic phase was concentrated to give 10.5 parts by weight of 2-(1-ethoxyaminobutylidene)-4-methoxycarbonyl-5-[tetrahydropyran-4-ylmethyl]-cyclohexane-1,3-dione (compound No. 1) as a viscous oil having the following structure: ##STR7##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04422864
Source datasetuspto-grants-1983_12
ORD IDord-60afa1e592894b7cb2838105b69a81f4
Source noteuspto-grants-1983_12