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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1801480Generated: October 31, 2026

Hydrochloric Acid → HCID 178450255, compound

https://huagongshe.com/reaction/1801480

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAnilineHCID 6115—
ReactantSodium AcetateHCID 517045—
ReactantSodium NitriteHCID 23668193—
Reactant2-Cyano-4-methoxy-5-n-butoxy phenylamineHCID 58367816—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 178450255HCID 17845025547.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

0.22 g (1 mmol) 2-cyano-4-methoxy-5-n-butoxyphenylamine and 3 mL (10 mol/L) hydrochloric acid were added into a round bottom flask. The solution was cooled to 0° C. and diazotized with sodium nitrite (0.072 g, 1 mmol) dissolved in water (1.0 mL), which was added dropwise to the solution. The mixture was stirred to react for 20 min. After adjusting the pH to 5˜6 with sodium acetate, the ethanol solution of aniline (0.093 g, 1 mmol) was added dropwise to the reaction mixture to react for 2 h under stirring, while maintaining the reaction temperature at between 0˜5° C., and using sodium acetate to keep the pH value at 5-6. The solution was kept overnight, filtered, and washed with water till colorless. The crude product was purified on a silica gel column with petroleum ether:ethyl acetate (v/v)=15:1 to yield 0.154 g of orange-yellow solid crystal product with a recovery rate of 47.5%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349835B2
Source datasetuspto-grants-2013_01
ORD IDord-5e12d0e9275f476a8a23e2716ffcee07
Source noteuspto-grants-2013_01