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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2118544Generated: October 31, 2026

O-ethylhydroxylamine hydrochloride → O-ethyl-N-(2,4,6-trichlorophenoxy)ethylhydroxylamine hydrochloride

https://huagongshe.com/reaction/2118544

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-ethylhydroxylamine hydrochlorideHCID 76850—
Reactant2-(2-Bromoethoxy)-1,3,5-trichlorobenzeneHCID 13565103—
SolventDiisopropylethylamineHCID 81531—
ProductO-ethyl-N-(2,4,6-trichlorophenoxy)ethylhydroxylamine hydrochlorideHCID 85519368105.9%

Reaction Conditions

Temperature50 °C

Reaction Steps

30.4 g (0.1 mole) of 2,4,6-trichlorophenoxyethyl bromide were added to a suspension of 48.5 g (0.5 mole) of O-ethylhydroxylamine hydrochloride in 250 ml of ethyldiisopropylamine, and the mixture was stirred for 4 days at 50° C. and then cooled to 15° C. and filtered under suction. The filtrate was evaporated down under reduced pressure, in the final stage at 60° C. and under 0.1 mbar, the residue was dissolved in 300 ml of ether, and the solution was gassed with hydrogen chloride at +3° C. 17 g of O-ethyl-N-(2,4,6-trichlorophenoxy)ethylhydroxylamine hydrochloride of melting point 173°-175° C. were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04678798
Source datasetuspto-grants-1987_07
ORD IDord-991487f18eba4c268c3883c4c47b1005
Source noteuspto-grants-1987_07