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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2039684Generated: November 1, 2026

Hydroxyamine hydrochloride → N-hydroxy-1-(4-methyl-1,2,5-thiadiazol-3-yl)-1-phenylmethanimine

https://huagongshe.com/reaction/2039684

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxyamine hydrochlorideHCID 443297—
Reactant(4-Methyl-1,2,5-thiadiazol-3-yl)(phenyl)methanoneHCID 11830534—
SolventPyridineHCID 1049—
ProductN-hydroxy-1-(4-methyl-1,2,5-thiadiazol-3-yl)-1-phenylmethanimineHCID 13635109099.6%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a stirred solution of (4-Methyl-[1,2,5]thiadiazol-3-yl)-phenyl-methanone (20 g, 98 mmol) in dry pyridine (70 mL) was added hydroxylamine hydrochloride (17 g, 245 mmol). The reaction mixture was stirred at 70° C. for 3 h, then concentrated in vacuo and diluted with ethyl acetate (100 mL) and water (100 mL). The organic layer was washed with water (2×100 mL) and dried over MgSO4. Evaporation of the solvent in vacuo afforded N-hydroxy-1-(4-methyl-1,2,5-thiadiazol-3-yl)-1-phenylmethanimine as an orange oil [24.3 g, yield 99.6%; HPLC/MS: m/z=220 (M+H); log P(HCOOH)=2.26].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580799B2
Source datasetuspto-grants-2013_11
ORD IDord-b3177ab24c444568863fd73d9c0d5201
Source noteuspto-grants-2013_11