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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722392Generated: November 1, 2026

Ethyl Acetate → HCID 13885857, compound

https://huagongshe.com/reaction/1722392

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium AcetateHCID 517045—
ReactantMethyl 2-((3-nitrophenyl)methylene)-3-oxobutanoateHCID 1536427—
Reactant(4-Methoxyphenyl)methyl carbamimidothioate--hydrogen chloride (1/1)HCID 13885856—
SolventDimethylformamideHCID 6228—
ProductHCID 13885857HCID 1388585779.5%

Reaction Conditions

Temperature65 °C

Reaction Steps

A solution of 2-[(3-nitrophenyl)methylene]-3-oxobutanoic acid, methyl ester (5.0 g, 0.02 mole) in 20 ml of dimethylformamide under argon at room temperature was treated with S-(4-methoxybenzyl)thiopseudourea, hydrochloride (4.65 g, 0.02 mole) and sodium acetate (1.64 g, 0.02 mole). The mixture was then heated at 65±5° C. for 3 hours. Upon cooling, ethyl acetate was added and a small amount of solids were filtered. The filtrate was washed with water (twice), aqueous sodium bicarbonate and saturated brine. The aqueous washes were extracted with fresh ethyl acetate. The combined filtrate and washings were dried (magnesium sulfate) and concentrated in vacuo to give about 9 g of crude product. Crystallization from acetone-isopropyl ether gave 6.8 g of product, melting point 125°-127.5° C., tlc, silica gel, ethyl acetate/hexane (1:1), Rf =0.48.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04855301
Source datasetuspto-grants-1989_08
ORD IDord-21144a38546d4933943783fb29ce70ae
Source noteuspto-grants-1989_08