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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1445334Generated: October 31, 2026

3-Benzyloxy-5-isopropyl-N-methoxy-N-methylthiophene-2-carboxamide → (3-Benzyloxy-5-isopropyl-thiophen-2-yl)-(4-methoxy-phenyl)-methanone

https://huagongshe.com/reaction/1445334

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Benzyloxy-5-isopropyl-N-methoxy-N-methylthiophene-2-carboxamideHCID 21961222—
ReactantHCID 178491912HCID 178491912—
SolventTetrahydrofuranHCID 8028—
Product(3-Benzyloxy-5-isopropyl-thiophen-2-yl)-(4-methoxy-phenyl)-methanoneHCID 21961226—

Reaction Conditions

Temperature22 °C

Reaction Steps

860 mg of 3-benzyloxy-5-isopropyl-N-methoxy-N-methylthiophene-2-carboxamide were dissolved in 50 ml of tetrahydrofuran (THF) and cooled to 0> C. in an ice bath, and 31.3 ml of 0.5 molar 4-methoxyphenymagnesium bromide solution in tetrahydrofuran were added. After 30 min, the ice bath was removed and the reaction mixture was warmed to 22° C. After one hour, 70 ml of saturated sodium bicarbonate solution were added to the reaction mixture, and it was extracted twice with 100 ml of methyl acetate each time. The combined organic phases were washed with 70 ml of saturated sodium chloride solution, dried over sodium sulfate and concentrated. The crude product was purified by column chromatography (SiO2, ethyl acetate/n-heptane=1:3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07666848B2
Source datasetuspto-grants-2010_02
ORD IDord-2c7f5dfa33924f98a20a2d63849e888f
Source noteuspto-grants-2010_02