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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274069Generated: October 30, 2026

Acetic Acid → HCID 14147965, compound

https://huagongshe.com/reaction/274069

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium ChlorideHCID 5234—
Reactant(Z)-1-(3-methoxyphenyl)-2-nitroetheneHCID 1809355—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 14147965HCID 1414796569%

Reaction Conditions

Temperature30 °C

Reaction Steps

A solution of (Z)-1-(3-methoxyphenyl)-2-nitroethene (33.85 g) in 1,4-dioxane (315 ml) was added dropwise to an efficiently stirred suspension of sodium borohydride (15.77 g) in a mixture of 1,4-dioxane (315 ml) and ethanol (98 ml) over a period of 0.5 hour while maintaining a temperature of 30° C. After stirring for 2 hours, the resultant slurry was diluted with ice water (393 ml) and the excess sodium borohydride was decomposed with 50% aqueous acetic acid (47.4 ml). To the solution, sodium chloride (68 g) and ethyl acetate were added. The organic layer was separated and the aqueous layer was extracted with ethyl acetate. The combined organic layer was washed with brine, dried over magnesium sulfate, and evaporated in vacuo. The residue was purified by distillation under reduced pressure to give 1-methoxy-3-(2-nitroethyl)benzene (23.62 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05387710
Source datasetuspto-grants-1995_02
ORD IDord-06dcae5850eb40f1a79735621668f9a1
Source noteuspto-grants-1995_02