HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 568664Generated: October 29, 2026
Ethyl bromoacetate → HCID 13015760, compound
https://huagongshe.com/reaction/568664
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 135589654 | HCID 135589654 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 13015760 | HCID 13015760 | — |
Reaction Steps
To a solution of 12 g of 7-chloro-6-hydroxy-3-(2,3-difluorophenyl)-1,2-benzisoxazole in 120 ml of DMF, 6.36 g of K2CO3 is added followed by 7.83 g of BrCH2CO2C2H5. The reaction is warmed at 60° C. for two hours and then allowed to stand for 18 hours. To the mixture 200 ml of water and 15 ml of 50% NaOH are added. The mixture is warmed at 90° C. for 90 minutes, poured into water and acidified. The product is extracted into ethylacetate which is dried over Na2SO4 and evaporated to give {[7-chloro-3-(2,3-difluorophenyl)-1,2-benzisoxazol-6-yl]oxy}acetic acid, mp 183°-187° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04728662 |
|---|
| Source dataset | uspto-grants-1988_03 |
|---|
| ORD ID | ord-8114a20dcec946588d20e8d0c2791d16 |
|---|
| Source note | uspto-grants-1988_03 |
|---|