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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1834729Generated: October 26, 2026

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

https://huagongshe.com/reaction/1834729

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 one 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 numberUS04071352
Source datasetuspto-grants-1978_01
ORD IDord-f5da47834b1d41a285217618e60a995a
Source noteuspto-grants-1978_01