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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-(4-methoxyphenyl)isoxazole-5-carboxylateHCID 776513—
SolventDichloromethaneHCID 6344—
SolventBoron tribromideHCID 25134—
ProductEthyl 3-(4-hydroxyphenyl)isoxazole-5-carboxylateHCID 13613384274.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340506B2
Source datasetuspto-grants-2016_05
ORD IDord-f8727927b39949abb06e4d09e49ae0ab
Source noteuspto-grants-2016_05