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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1808860Generated: November 2, 2026

Hydrochloric Acid → 3-(2-Methoxyphenyl)-5-methyl-1,2-oxazole-4-carboxylic acid

https://huagongshe.com/reaction/1808860

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl EtherHCID 3283—
ReactantSodium HydroxideHCID 14798—
ReactantETHYL 3-(2-METHOXYPHENYL)-5-METHYLISOXAZOLE-4-CARBOXYLATEHCID 10999825—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product3-(2-Methoxyphenyl)-5-methyl-1,2-oxazole-4-carboxylic acidHCID 6484100—

Reaction Conditions

Temperature65 °C

Reaction Steps

The reaction mixture of ethyl 3-(2-methoxyphenyl)-5-methylisoxazole-4-carboxylate (12.85 g, 49.2 mmol) and sodium hydroxide (9.84 g, 246 mmol) in MeOH (100 mL) and Water (10 mL) in a 500-mL round bottom flask was stirred at 65° C. for 20 hours. The MeOH was removed in vacuo, then the concentrated reaction mixture was transferred to a 500-mL separatory funnel with 150 mL of water and 100 mL of ether. The organic layer was discarded. The aqueous layer was acidified by adding concentrated HCl (26 mL). The product precipitated and was separated by filtration and dried under high vacuum to give 10.63 g (93%, theoretical yield 11.47 g). 1H NMR (400 MHz, CD3OD) δ 2.69 (s, 3H, CH3), 3.77 (s, 3H, OCH3), 7.00-7.07 (m, 2H, aryl), 7.32-7.34 (m, 1H, aryl), 7.43-7.48 (m, 1H, aryl).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362004B2
Source datasetuspto-grants-2013_01
ORD IDord-1845599ebd854fc8805a7a3ff01f3896
Source noteuspto-grants-2013_01