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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 414698Generated: October 26, 2026

Ethyl-alpha-carbethoxy-4-dimethylamino-2-nitrocinnamate → Ethyl-alpha-carbethoxy-4-methylamino-2-nitrocinnamate

https://huagongshe.com/reaction/414698

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl-alpha-carbethoxy-4-dimethylamino-2-nitrocinnamateHCID 14365894—
ReactantHCID 178418268HCID 178418268—
SolventAcetic AcidHCID 176—
ProductEthyl-alpha-carbethoxy-4-methylamino-2-nitrocinnamateHCID 53938328—

Reaction Steps

The cinnamic ester (1) (5.0 g, 14.8 mmol) was dissolved in 100 mL of acetic acid and 7.6 g (17.2 mmol) of lead tetracetate was added. After allowing the mixture to stir for one hour at room temperature, the solvent was removed. Toluene (100 mL) was added and the slurry concentrated, then 100 mL of chloroform (CHCl3) was added, the solid broken up thoroughly, and the solution decanted. Chloroform (100 mL) was added to the solid and the mixture refluxed briefly, filtered, and the filtrate combined with the previous CHCl3 solution. After concentrating the organic solution the residue was chromatographed on 350 g of silica gel eluting with 1:19 (v/v) acetone:CHCl3. Fractions 83-140 (15 mL/fraction) were combined and concentrated to yield the product which was crystallized from CH2Cl2 (3.45 g, 72%), m.p. 113°-114° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04794079
Source datasetuspto-grants-1988_12
ORD IDord-101b99fa3d5c470e8269a6c91a0239e3
Source noteuspto-grants-1988_12