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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1834738Generated: October 26, 2026

O-Methylhydroxylamine → N-methoxy-2,4,5-trichlorobenzenesulfonamide

https://huagongshe.com/reaction/1834738

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-MethylhydroxylamineHCID 4113—
ReactantSodium HydroxideHCID 14798—
Reactant2,4,5-Trichlorobenzenesulfonyl chlorideHCID 27575—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductN-methoxy-2,4,5-trichlorobenzenesulfonamideHCID 20324727—

Reaction Steps

5.0 g. of methoxy amine was dissolved in 100 ml. of H2O. Then, 14.0 g. of 2,4,5-trichlorobenzene sulfonyl chloride dissolved in 25 ml. of tetrahydrofuran was added under high speed mechanical stirring. Then, 8.8 g. of sodium hydroxide in a 50% solution + 10 ml. of water was dropped in at room temperature. An exothermic reaction took place and the temperature went up to 37.5° C. When the reaction subsided, it was stirred at room temperature for two hours and the solid was then filtered off and stirred into 150 ml. of ether for 1 hour. The solid was removed by filtration to yield 11.3 g. of product. The product was redissolved in ether. The ether was evaporated to yield 7.4 g. of product, m.p. 163°-166° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04071350
Source datasetuspto-grants-1978_01
ORD IDord-5fa5b5ce5e27428fadb3945f27866816
Source noteuspto-grants-1978_01