HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 414352Generated: October 29, 2026
Hydroxyamine hydrochloride → HCID 86742619, compound
https://huagongshe.com/reaction/414352
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | HCID 14348782 | HCID 14348782 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 86742619 | HCID 86742619 | 100.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04791209 |
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| Source dataset | uspto-grants-1988_12 |
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| ORD ID | ord-f639f6d420a34fce9e8f28142bb0a46d |
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| Source note | uspto-grants-1988_12 |
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