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
Participants
| Role | Name | HCID | Charge |
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| Reactant | O-ethylhydroxylamine hydrochloride | HCID 76850 | — |
| Reactant | 2-(2-Bromoethoxy)-1,3,5-trichlorobenzene | HCID 13565103 | — |
| Solvent | Diisopropylethylamine | HCID 81531 | — |
| Product | O-ethyl-N-(2,4,6-trichlorophenoxy)ethylhydroxylamine hydrochloride | HCID 85519368 | 105.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04678798 |
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| Source dataset | uspto-grants-1987_07 |
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| ORD ID | ord-991487f18eba4c268c3883c4c47b1005 |
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| Source note | uspto-grants-1987_07 |
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