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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 597192Generated: October 30, 2026

Ethyl 3-(3,4-dimethoxyanilino)but-2-enoate → Ethyl 3-(3,4-dimethoxyanilino)butanoate

https://huagongshe.com/reaction/597192

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-(3,4-dimethoxyanilino)but-2-enoateHCID 70638975—
CatalystPlatinum oxide (PtO)HCID 82844—
SolventAcetic AcidHCID 176—
SolventChloroformHCID 6212—
ProductEthyl 3-(3,4-dimethoxyanilino)butanoateHCID 2143973499.2%

Reaction Steps

A mixture of 30.0 g of the product of Example 1 (m.p. 59°-60°), and 2.0 g of platinum oxide in 250 ml of acetic acid was hydrogenated in a Paar shaker at 50 p.s.i.; reduction was complete in 1 hr. The mixture was filtered and concentrated under reduced pressure, to give an amber oil which was dissolved in chloroform and washed with sodium bicarbonate solution followed by saturated sodium chloride. The organic layer was dried over magnesium sulfate and concentrated under reduced pressure to give 30.0 g of an amber oil which was used in the next step without further purification. A sample of oil was converted to the hydrochloride salt, m.p. 137.5°-139°. An equivalent sample of the hydrochloride salt (m.p. 138°-139.5°) was analyzed.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04013662
Source datasetuspto-grants-1977_03
ORD IDord-c38154bd80bf48879b2262a20f99b05a
Source noteuspto-grants-1977_03