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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 414699Generated: October 30, 2026

Acetic Acid → Ethyl-alpha-carbethoxy-4-methylamino-2-nitrodihydrocinnamate

https://huagongshe.com/reaction/414699

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium borohydrideHCID 4311764—
ReactantEthyl-alpha-carbethoxy-4-methylamino-2-nitrocinnamateHCID 53938328—
SolventEthanolHCID 702—
ProductEthyl-alpha-carbethoxy-4-methylamino-2-nitrodihydrocinnamateHCID 2128018691%

Reaction Steps

Sodium borohydride (NaBH4) (0.2 g, 5.8 mmol) was added to a slurry of the cinnamic ester (2) (3.4 g, 10.5 mmol) in 100 mL of absolute ethanol and the reaction allowed to stir at room temperature for 1.5 hours. Acetic acid (0.5 mL) was added and the mixture concentrated. The residue was dissolved in 250 mL of CHCl3 and was washed with 100 mL of saturated sodium bicarbonate (NaHCO3) solution, and H2O (100 mL). The organic phase was separated, dried (Na2SO4) and concentrated to produce 3.1 g of an orange solid. An analytical sample was obtained by crystallization from methanol(MeOH)-water, m.p. 75°-77° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04794079
Source datasetuspto-grants-1988_12
ORD IDord-29c1c848a65341189ec72c6c6ec52684
Source noteuspto-grants-1988_12