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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1065286Generated: October 30, 2026

Ethanol → HCID 12833329, compound

https://huagongshe.com/reaction/1065286

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 86738367HCID 86738367—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductHCID 12833329HCID 12833329—

Reaction Conditions

Temperature40 °C

Reaction Steps

22 g. (76.5 mmol.) of 2-(4'-chloro-β-aminostyryl)nicotinic acid N-methylamide (Compound XIX) were dissolved in 80 ml. of tetrahydrofuran and 40 ml. of ethanol and a mixture of 40 ml. of acetic acid and 40 ml. of water was added. The reaction mixture was stirred at 40° C. for 4 hours. The reaction mixture was then made basic to pH 9 with sodium hydroxide solution and extracted with diethyl ether, ethyl acetate and methylene chloride. The three organic extracts were combined, treated with charcoal, dried over anhydrous magnesium sulfate and concentrated at reduced pressure to obtain a yellow solid which was recrystallized from ethanol to obtain the product as a yellow green solid, m.p. 162°-163° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04329349
Source datasetuspto-grants-1982_05
ORD IDord-b5222bbff40245f3a00c25170ca13bd0
Source noteuspto-grants-1982_05