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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1871532Generated: October 26, 2026

N-methoxy-N-methyl-3-(3-cyclopentyloxy-4-methoxyphenyl)prop-2-enamide → HCID 21193738, compound

https://huagongshe.com/reaction/1871532

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methoxy-N-methyl-3-(3-cyclopentyloxy-4-methoxyphenyl)prop-2-enamideHCID 54075299—
ReactantHCID 178418348HCID 178418348—
SolventHydrochloric AcidHCID 313—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21193738HCID 2119373897%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of N-methoxy-N-methyl-3-(3-cyclopentyloxy-4-methoxyphenyl)prop-2-enamide (1.986 g, 6.50 mmol) in dry tetrahydrofuran (15 ml) at -78° C. was added methyl lithium (1.4M solution in hexanes, 10.20 ml, 14.3 mmol) dropwise over 3 minutes. The resulting solution was stirred for 1 hour at 0° C., after which time the reaction mixture was diluted with 5% HCl in methanol (20 ml) at 0° C., and partitioned between brine (35 ml) and an equal volume of methylene chloride and diethyl ether (100 ml). The organics were dried (Na2SO4) and concentrated in vacuo to give a light yellow oil. The oil was purified by flash chromatography (SiO2 ; ethyl acetate/hexane (35:65)) to afford the title compound as a colorless oil (1.642 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06103749
Source datasetuspto-grants-2000_08
ORD IDord-b90467da69d345e3a9658cfd5033c664
Source noteuspto-grants-2000_08