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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339455Generated: October 29, 2026

Water → HCID 59016634, compound

https://huagongshe.com/reaction/339455

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
Reactant2-Ethyl-3-methoxybenzoyl chlorideHCID 22144562—
ReactantHCID 59016633HCID 59016633—
SolventTolueneHCID 1140—
SolventChloroformHCID 6212—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
ProductHCID 59016634HCID 5901663429%

Reaction Steps

A 20% aqueous solution of NaOH (275 mg, 1.37 mmol) was added to a solution of 3-(3,5-dimethyl-phenyl)-5,5-dimethyl-[1,2,4]oxadiazol-4-ylamine (200 mg, 0.91 mmol) in 2 mL of toluene. 2-Ethyl-3-methoxybenzoyl chloride (199 mg, 1 mmol) was then added to the mixture. The reaction was stirred at room temperature for 2 hours, and then heated at 50° C. for 1 hour. TLC indicated 3 spots. Water, dilute NaOH, and CHCl3 were then added to the reaction mixture. The organic phase was separated, dried over MgSO4, and the solvent removed in vacuo. The residue was triturated with 10% ether in hexane. Filtration and air-drying of the resultant solid provided 100 mg (29% 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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895306B2
Source datasetuspto-grants-2014_11
ORD IDord-a6a9aaabc1f749e8b60be8a6db26f836
Source noteuspto-grants-2014_11