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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389934Generated: October 29, 2026

Methanol → 5-[2,4-Bis(benzyloxy)-5-chlorophenyl]-isoxazole-3-carboxylic acid

https://huagongshe.com/reaction/389934

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantLithium HydroxideHCID 3939—
ReactantEthyl 5-(2,4-bis(benzyloxy)-5-chlorophenyl)isoxazole-3-carboxylateHCID 24774040—
SolventWaterHCID 962—
Product5-[2,4-Bis(benzyloxy)-5-chlorophenyl]-isoxazole-3-carboxylic acidHCID 67083506—

Reaction Steps

A mixture of ethyl 5-(2,4-bis(benzyloxy)-5-chlorophenyl)isoxazole-3-carboxylate (200 mg, 0.43 mmol), methanol (10 ml), water (6-7 ml), and LiOH (16 mg, 0.65 mmol) was allowed to stand at 50-60° C. for 24 h. The solution was concentrated under vacuo to remove methanol, and the remaining aqueous solution was extracted with Et2O to remove traces of unreacted starting material. The aqueous solution was acidified with 1 M HCl and extracted with three portions of AcOEt. The combined organic extracts were washed with saturated aqueous sodium chloride and dried over sodium sulfate. Removal of the solvent under reduced pressure afforded a residue, which was chromatographed on silica gel (DCM/methanol: 9/1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383616B2
Source datasetuspto-grants-2013_02
ORD IDord-bcc4e13204e74a96a6176b2e9e70084c
Source noteuspto-grants-2013_02