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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 414352Generated: October 29, 2026

Hydroxyamine hydrochloride → HCID 86742619, compound

https://huagongshe.com/reaction/414352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantHCID 14348782HCID 14348782—
SolventPyridineHCID 1049—
ProductHCID 86742619HCID 86742619100.3%

Reaction Steps

A mixture of 5-(3-chlorobenzoyl)-4,7-dichloro-2,3-dihydrobenzo[b]furan-2-carboxylic acid (11.5 g), hydroxylamine hydrochloride (21.5 g) and pyridine (110 ml) was refluxed for 14 hours. After distilling off the solvent, water was added to the mixture which then was rendered acidic with HCl and subjected to extraction with ether. The ether layer was washed with water an.d dried. By distilling off the solvent, 12 g of 5-(3-chloro-α-hydroxyiminobenzyl)4,7-dichloro-2,3-dihydrobenzo[b]furan-2-carboxylic acid was obtained. This compound (12 g) was dissolved in anhydrous dimethylformamide (150 ml), and to the ice-cooled solution, 3.9 g of 60% sodium hydride was added in small amounts under agitation. After stirring for 8 hours at room temperature, the mixture was left to stand overnight. After adding water, the mixture was rendered acidic with HCl and subjected to extraction with ether. The ether layer was washed with water and dried. After distilling off the solvent, the residue was recrystallized from acetone-water, yielding 5.6 g of 5-chloro- 3-(3-chlorophenyl)-7,8-dihydrofuro[2,3-g]-1,2-benzisoxazole-7-carboxylic acid. m.p. 168°-169° C. This compound exhibited a mass spectrum having a molecular ion peak at m/e 349.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04791209
Source datasetuspto-grants-1988_12
ORD IDord-f639f6d420a34fce9e8f28142bb0a46d
Source noteuspto-grants-1988_12