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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241579Generated: October 25, 2026

Hydrochloric Acid → HCID 178518989, compound

https://huagongshe.com/reaction/241579

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantNitrogenHCID 947—
ReactantThionyl ChlorideHCID 24386—
Reactant4-chloro-N,2-dihydroxybenzamideHCID 2781848—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178518989HCID 17851898989.8%

Reaction Conditions

Temperature30 °C

Reaction Steps

4-chloro-N,2-dihydroxy-benzamide (8 g, 42.7 mmol) is added to 10 ml of tetrahydrofuran under coverage of N2, while maintaining the temperature inside vessel lower than 30° C. and thereto is drop-added slowly 10 ml of SOCl2. After completion of drop-addition, the reaction is stirred for 30 minutes and evaporated to dryness. The residual SOCl2 is removed by azeotropic distillation with anhydrous benzene. The reaction is evaporated to dryness to obtain a yellow powder, which is dissolved in 10 ml of dioxane, while maintaining the temperature inside vessel at lower than 30° C., and thereto is drop-added slowly 5 ml of Et3N and stirred for 30 minutes, then thereto is drop-added 10% hydrochloric acid to pH=2. Under stirred, a large amount of light yellow deposit precipitates and is filtered out and recrystallized in methanol to obtain 6.50 g of 3-hydroxy-6-chloro-benzisoxazole, with a yield of 89%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653069B2
Source datasetuspto-grants-2014_02
ORD IDord-00d57327d2284c72a0b8ce2b3d58fa3e
Source noteuspto-grants-2014_02