HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 524415Generated: October 31, 2026
Ethyl 3-(4-methoxyphenyl)isoxazole-5-carboxylate → Ethyl 3-(4-hydroxyphenyl)isoxazole-5-carboxylate
https://huagongshe.com/reaction/524415
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 3-(4-methoxyphenyl)isoxazole-5-carboxylate | HCID 776513 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Boron tribromide | HCID 25134 | — |
| Product | Ethyl 3-(4-hydroxyphenyl)isoxazole-5-carboxylate | HCID 136133842 | 74.3% |
Reaction Steps
To a stirred solution of ethyl 3-(4-methoxyphenyl)isoxazole-5-carboxylate (1 g, 4.04 mmol, prepared according to literature method Tet. Lett 2009, 50(27), 3948-3951) in 8 mL DCM, Boron tribromide 1 M solution in DCM (8.0 mL, 8.08 mmol) was added dropwise at −78° C. After complete addition reaction mixture was allowed to warm slowly and further stirred for 16 hrs at RT. After completion of the reaction, solvent was removed under reduced pressure. The reaction mixture was diluted with ice cold water (20 mL) and extracted with ethyl acetate (3×50 mL). The combined organic layer was washed with water, brine and dried over sodium sulfate, filtered and concentrated under reduced pressure to get ethyl 3-(4-hydroxyphenyl)isoxazole-5-carboxylate (0.7 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09340506B2 |
|---|
| Source dataset | uspto-grants-2016_05 |
|---|
| ORD ID | ord-f8727927b39949abb06e4d09e49ae0ab |
|---|
| Source note | uspto-grants-2016_05 |
|---|