HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 568644Generated: October 30, 2026
Ethyl bromoacetate → HCID 13015695, compound
https://huagongshe.com/reaction/568644
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 135589642 | HCID 135589642 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 13015695 | HCID 13015695 | — |
Reaction Steps
7-chloro-6-hydroxy-3-(2-pyridyl)-1,2-benzisoxazole (10.0 g) is dissolved in 80 ml of DMF and added to an ice cold suspension of NaH (1.1 g) in 50 ml of DMF. When hydrogen evolution ceases, ethyl bromoacetate (7.5 g) in 20 ml of DMF is added. After an additional 90 minutes, 200 ml of H2O and 10 ml of 50% NaOH are added and the reaction warmed at 65° C. for 45 minutes. The mixture is poured into H2O, acidified to pH 1-2, and a solid product filtered and dried to give {[7-chloro-3-(2-pyridyl)-1,2-benzisoxazole-6-yl]oxy}acetic acid, mp 255°-256° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04728662 |
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| Source dataset | uspto-grants-1988_03 |
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| ORD ID | ord-102ad08aa569468780a3f3656fd12b54 |
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| Source note | uspto-grants-1988_03 |
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