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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339456Generated: October 30, 2026

Water → HCID 59016634, compound

https://huagongshe.com/reaction/339456

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
Reactant2-Ethyl-3-methoxybenzoyl chlorideHCID 22144562—
ReactantHCID 59016633HCID 59016633—
SolventTolueneHCID 1140—
SolventChloroformHCID 6212—
ProductHCID 59016634HCID 5901663440%

Reaction Steps

A 5% aqueous solution of NaOH (4 mL) was added to a solution of 3-(3,5-dimethyl-phenyl)-5,5-dimethyl-[1,2,4]oxadiazol-4-ylamine (90 mg) in 6 mL of toluene. 2-Ethyl-3-methoxybenzoyl chloride (140 mg) was then added to the mixture. The reaction was stirred at room temperature for 30 hours. Water and CHCl3 were added. The organic phase was separated, dried over MgSO4, and the solvent was removed in vacuo. The residue was triturated with 100 mL of 10% ether in hexane by magnetic stirring of the mixture in a vessel for 1 hour. Filtration and air-drying of the resultant solid provided 62 mg (40% yield) of N-[3-(3,5-dimethyl-phenyl)-5,5-dimethyl-[1,2,4]oxadiazol-4-yl]-2-ethyl-3-methoxy-benzamide. 1H-NMR (300 MHz, CDCl3) δ (ppm): 7.42 (s, 2H), 7.11 (s, 1H), 7.11 (t, 1H), 6.9 (d, 1H), 6.67 (d, 1H), 3.81 (s, 3H), 2.55 (q, 2H), 2.34 (s, 6H), 1.7 (br s, 6H), 1.05 (t, 3H), Rf=0.5 (1:1 ethyl acetate:hexane). The filtrate contained an additional quantity of the intended product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895306B2
Source datasetuspto-grants-2014_11
ORD IDord-b5ca3d8497e24a80ae7997d4f1ca4dd6
Source noteuspto-grants-2014_11