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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433183Generated: October 26, 2026

4-Bromobenzene-1,2-diamine → HCID 178506219, compound

https://huagongshe.com/reaction/1433183

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromobenzene-1,2-diamineHCID 323593—
ReactantHCID 69042140HCID 69042140—
SolventEthanolHCID 702—
ProductHCID 178506219HCID 17850621997.7%

Reaction Steps

A 5-L 4-neck round bottom flask equipped with a thermocouple, mechanical stirrer and an argon inlet adapter was charged with 4-bromo-1,2-phenylenediamine (166.4 g, 0.863 mol), ethanol (2 L), followed by the addition of 2-(4-trifluoromethyl-phenoxy)-acetimidic acid ethyl ester hydrochloride (272.0 g, 0.959 mol) and ethanol (0.9 L). The initial solution of diamine turned to a suspension upon the addition of 2-(4-trifluoromethyl-phenoxy)-acetimidic acid ethyl ester hydrochloride, and an exotherm from 17° C. to 28° C. was noted. The reaction was assayed at 2.5 h and found to be complete. The reaction was filtered though Celite (60 g) and the gray solid was washed with ethanol (200 mL) until the filtrates were no longer colored. A clean 12-L 4-neck round bottom flask equipped with a mechanical stirrer, a 1-L addition funnel and ice bath for cooling was set-up and the ethanol filtrates were transferred into the 12-L flask. While cooling the flask, water (3.5 L) was added to the ethanol, and the resulting brown suspension was stirred for 1 h in the ice bath to enhance recovery. The brown solid was filtered evenly between two Buchner funnels, each washed with cold water (150 mL, 2×200 mL), and the brown solid was air-dried for a few hours. The brown solid was transferred to two amber bottles, dried in a hi-vac oven (60 mm) at 60° C., to a constant weight and afforded a total of 331.9 g (103% isolated yield; 97.7-98%, HPLC area %) of the title compound as a brown powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612211B2
Source datasetuspto-grants-2009_11
ORD IDord-02e3c77fd39d4743b42a20094edda923
Source noteuspto-grants-2009_11