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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 487657Generated: October 29, 2026

3,4-Dimethylaniline → HCID 53651546, compound

https://huagongshe.com/reaction/487657

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-DimethylanilineHCID 7248—
ReactantSodium AcetateHCID 517045—
ReactantHCID 10611783HCID 10611783—
ReactantSodium NitriteHCID 23668193—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
ProductHCID 53651546HCID 5365154670%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of sodium nitrite (0.414 g) in water (2.0 ml) was dropwise added to a solution of 3,4-xylidine (0.61 g) in concentrated hydrochloric acid (1.5 ml) at a temperature of 0° C., followed by stirring for 30 minutes at 0° C. To the mixture were added sodium acetate (1.23 g) and methyl 2-(3,4-dimethoxybenzyl)acetoacetate (1.33 g). After stirring for an hour at room temperature, the reaction mixture was poured into water and extracted with ethyl ether. The ethereal layer was washed with a saturated sodium hydrogencarbonate aqueous solution and water, dried (MgSO4) and concentrated under reduced pressure. The residue was dissolved in methanol (20 ml), to which 1N-KOH methanolic solution (5 ml) was dropwise added at 0° C. After stirring for an hour at 0° C., the resultant mixture was neutralized with acetic acid and poured into water. The precipitate was collected by filtration and recrystallized from acetone-methanol to give methyl 3-(3,4-dimethoxyphenyl)-2-(3,4 -dimethylphenylhydrazino)propionate (1.25 g, 70%) as pale red prisms.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05296499
Source datasetuspto-grants-1994_03
ORD IDord-37a1ed42424d453d8e04651b14aadc7b
Source noteuspto-grants-1994_03