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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1517753Generated: October 26, 2026

Hydrochloric Acid → 2-(Hydroxymethyl)-4-methoxy-6-((2-nitro-4-(trifluoro-methyl)-phenyl)diazenyl)-phenol

https://huagongshe.com/reaction/1517753

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantBenzenamine, 2-nitro-4-(trifluoromethyl)-HCID 67865—
Reactant2,6-Bis(hydroxymethyl)-4-methoxyphenolHCID 827459—
ReactantSodium NitriteHCID 23668193—
CatalystSulfamic AcidHCID 5987—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-(Hydroxymethyl)-4-methoxy-6-((2-nitro-4-(trifluoro-methyl)-phenyl)diazenyl)-phenolHCID 13612339142.4%

Reaction Steps

In a 500 ml round bottom flask equipped with a magnetic stirrer was added 19.9 g 2-nitro-4-(trifluoromethyl)-aniline (96.5 mmol) (Aldrich, Milwaukee, Wis.), 41 ml concentrated HCl (aq), 100 ml deionized water, 100 ml ethanol, and 80 ml THF. The suspension was stirred for 30 minutes and 7.07 g sodium nitrite (102 mmol) in 30 ml water was added dropwise over 60 minutes while keeping the reaction mixture at 0° C. The reaction mixture was stirred for an additional 1 hour. 300 mg Sulfamic acid was added to destroy excess nitrite. The mixture was filtered to remove undissolved solids. The filtered diazonium mixture along with a solution of sodium hydroxide (15.1 g in 100 ml water) were added dropwise to a solution containing 19.7 g (2-hydroxy-5-methoxy-1,3-phenylene)dimethanol (107 mmol), 4.3 sodium hydroxide, 200 ml deionized water, and 50 ml THF at 0° C. The reaction mixture was allowed to stir at 0° C. for 1 hour and room temperature for 4 hours. The mixture was poured into 3 liters water. The mixture was acidified to pH 3-4. The dark crude product was filtered and washed with several liters of water to generate a dark solid which was dried under high vacuum at 55° C. for 72 hours to give 15.2 g (42% yield) product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08232326B2
Source datasetuspto-grants-2012_07
ORD IDord-99ce06827e0e4f1e923360d5acc91bd2
Source noteuspto-grants-2012_07