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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1407103Generated: October 25, 2026

Hydrochloric Acid → HCID 178496277, compound

https://huagongshe.com/reaction/1407103

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant3-(Trifluoromethyl)anilineHCID 7375—
ReactantMethyl 4-methoxyacetoacetateHCID 123500—
ReactantSodium AcetateHCID 517045—
ReactantSodium NitriteHCID 23668193—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 178496277HCID 17849627788%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of NaNO2 (4.14 g, 60 mmol) in H2O (15 mL) was added dropwise at 0° C. to a mixture of 3-(trifluoromethyl)aniline (6.24 mL, 50 mmol) and 6 M HCl aqueous solution (50 mL, 300 mmol). After stirring for 15 min, the resulting aqueous solution was added to a suspension of methyl 4-methoxyacetoacetate (7.31 mL, 50 mmol) and NaOAc (24.6 g, 300 mmol) in EtOH (80 mL) pre-cooled at 0° C. The precipitate was collected by filtration, washed with water, and dissolved in AcOEt. The organic solution was washed with water and brine, dried over Na2SO4, and concentrated under reduced pressure. The residue was crystallized from hexane/AcOEt to give the title compound (14.0 g, 88% yield) as pale yellow crystals: 1H NMR (300 MHz, CDCl3): δ ppm 3.51 (3H×0.36, s), 3.52 (3H×0.64, s), 3.90 (3H×0.36, s), 3.94 (3H×0.64, s), 4.68 (2H×0.64, s), 4.70 (2H×0.36, s), 7.41-7.59 (3H+1H×0.64, m), 7.71 (1H×0.36, s), 13.00 (1H×0.64, s), 14.87 (1H×0.36, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916566B2
Source datasetuspto-grants-2014_12
ORD IDord-5675ac85c1eb40398ebe7e36ed11cce9
Source noteuspto-grants-2014_12