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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016117Generated: November 1, 2026

Sodium Hydroxide → 3-Methyl-2-(5-phenyl-1,3,4-oxadiazol-2-ylamino)butanoic acid

https://huagongshe.com/reaction/1016117

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 3-methyl-2-(5-phenyl-1,3,4-oxadiazol-2-ylamino)butanoateHCID 57888933—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product3-Methyl-2-(5-phenyl-1,3,4-oxadiazol-2-ylamino)butanoic acidHCID 5788925750%

Reaction Steps

Crude ethyl 3-methyl-2-(5-phenyl-1,3,4-oxadiazol-2-ylamino)butanoate (assumed 5 mmol) was dissolved in a mixture of THF (10 ml) and MeOH (2 ml) and then treated dropwise (exothermic) with aqueous 1 N NaOH (6 mL) solution. The reaction was stirred for 1 h, diluted with H2O (50 mL) and then extracted with Et2O (1×50 mL). The aqueous layer was acidified to pH 3 with aqueous 1N HCl solution and then extracted with EtOAc (3×35 mL). The EtOAc extracts were combined, washed with sat. aqueous NaCl solution, dried (MgSO4) and the solvent was removed in vacuo to give 3-methyl-2-(5-phenyl-1,3,4-oxadiazol-2-ylamino)butanoic acid in 50-75% yield over 3 steps in purity >90% as judged by LCMS. MS found: 262 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07985861B2
Source datasetuspto-grants-2011_07
ORD IDord-e4636c65bb2c410d8e871def10281314
Source noteuspto-grants-2011_07