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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1275519Generated: November 3, 2026

Ammonium Chloride → HCID 22117030, compound

https://huagongshe.com/reaction/1275519

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 22326083HCID 22326083—
CatalystIronHCID 23925—
SolventIsopropanolHCID 3776—
ProductHCID 22117030HCID 2211703035.8%

Reaction Steps

2-Nitro-1,3,5-triethoxybenzene (12.8 g) in isopropyl alcohol (80 ml) was reacted at 90° C. for 2 hours with an iron powder (28 g) and aqueous ammonium chloride solution (2.85 g/water 8.4 ml). This mixture was extracted with ethyl acetate and the solvent of the extract was distilled off. To the resulting solution was further added conc. hydrochloric acid (6 ml), and the mixture was washed with a small amount of aceton to obtain 2,4,6-triethoxyaniline hydrochloride (4.7 g). 2,4,6-Triethoxyaniline hydrochloride (2.6 g) was dissolved in methanol (50 ml) , and the solution was acidified with conc. hydrochloric acid (3.5 ml). Then, aqueous sodium nitrite solution (1.4 g/water 10 ml) was added slowly to this solution while cooling with ice. Two hours later, 2-hydroxy-4-methoxybenzophenone-5-sulfonic acid (6.2 g) was added to the solution. One hour later, this mixture was extracted with methylene chloride, and the extract was washed with water. Then, the solvent of the resulting solution was distilled off to obtain 2,4,6-triethoxybenzenediazonium 2-hydroxy-4-methoxybenzophenone-5-sulfonate (4.5 g) as a pale yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06162574
Source datasetuspto-grants-2000_12
ORD IDord-7d28c5c11acf48adbcc946d6f3f1958e
Source noteuspto-grants-2000_12