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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154585Generated: October 30, 2026

Hydroxyamine hydrochloride → HCID 13343677, compound

https://huagongshe.com/reaction/1154585

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantHCID 12747895HCID 12747895—
SolventPyridineHCID 1049—
ProductHCID 13343677HCID 1334367732.3%

Reaction Steps

Hydroxylamine hydrochloride (15.19 g, 0.2186 mol.) and (3a) (10.84 g., 0.0322 mol.) were heated at reflux in 75 ml. of dry pyridine for 5 hours. On cooling, the pyridine was removed on a rotary evaporator and chased with ethanol. The residue, a yellow gum, was taken up in ethyl acetate and washed with dilute aqueous hydrochloric acid and brine, then dried over anhydrous magnesium sulfate and evaporated to a gum containing both E and Z isomers of the oxime. Without further purification, the gum was taken up in 20 ml. of absolute ethanol and treated with 120 ml. of 1M alcoholic potassium hydroxide at reflux on a steam bath for 3 hours then refrigerated at 0°-5° C. for 48 hours. The resulting precipitate was collected by filtration, washed with hexane, dried, and dissolved in 300 ml. warm distilled water. Acidification to pH 2.0 by addition of 4.0 M aqueous hydrochloric acid gave a gelatinous precipitate which was extracted into ethyl acetate, dried with anhydrous magnesium sulfate, decolorized with Darco, and evaporated. Recrystallization from ethyl acetate with hexane afforded the furobenzisoxazole (4a) in 32.3% yield, m.p. 214°-215° C. Analysis (C16H10ClNO4) C,H,N,Cl.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04490384
Source datasetuspto-grants-1984_12
ORD IDord-2fa49e0de4c741d5aa13a3b5fdb506f6
Source noteuspto-grants-1984_12