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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1691514Generated: November 3, 2026

Hydrochloric Acid → HCID 136348288, compound

https://huagongshe.com/reaction/1691514

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
ReactantSodium HydroxideHCID 14798—
ReactantBenzenamine, 2-nitro-4-(trifluoromethyl)-HCID 67865—
ReactantSodium NitriteHCID 23668193—
CatalystSulfamic AcidHCID 5987—
SolventWaterHCID 962—
ProductHCID 136348288HCID 13634828876%

Reaction Conditions

Temperature0 °C

Reaction Steps

In a 500 ml round bottom flask equipped with a magnetic stirrer was combined 26.0 g (126 mmol) 2-nitro-4-(trifluoromethyl)-aniline, 53 ml conc. HCl, 100 ml deionized water, and 150 ml ethanol. The mixture was cooled to 0° C. and sodium nitrite in 30 ml water was added dropwise over 60 minutes. The reaction mixture was stirred for an additional 1 hour and 300 mg sulfamic acid was added to destroy the excess nitrite. The solids were filtered and the cold filtrate was set aside. In a 1 liter flask was suspended (2-hydroxy-5-methoxy-1,3-phenylene)dimethanol in 200 ml deionized water and 100 ml ethanol. Approximately one-fourth of a solution of sodium hydroxide (25.4 g, 635 mmol) in 100 ml water was added to the phenolic mixture at 0° C. The diazonium salt mixture and remaining sodium hydroxide solution were added concurrently to the phenolic mixture over 1 hour. The reaction mixture was allowed to stir at 0° C. for 1 hour and room temperature for 4 hours. The mixture was poured in 3 liters water and the pH adjusted to 3-4 using 1N HCl. The solid was filtered and washed with ample amounts of water and then vacuum dried (0.1 mm Hg) at 55° C. for 40 hours to give 27.4 g (76%) of a red solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153703B2
Source datasetuspto-grants-2012_04
ORD IDord-1778c2c3c2b04aa29d8eb3be0e82a4e9
Source noteuspto-grants-2012_04