HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241579Generated: October 25, 2026
Hydrochloric Acid → HCID 178518989, compound
https://huagongshe.com/reaction/241579
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 4-chloro-N,2-dihydroxybenzamide | HCID 2781848 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 178518989 | HCID 178518989 | 89.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08653069B2 |
|---|
| Source dataset | uspto-grants-2014_02 |
|---|
| ORD ID | ord-00d57327d2284c72a0b8ce2b3d58fa3e |
|---|
| Source note | uspto-grants-2014_02 |
|---|