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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1446982Generated: October 30, 2026

Water → 3-Ethyl-5-(2-methoxyethoxymethoxyphenyl)-2-cyclohexenone

https://huagongshe.com/reaction/1446982

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3-Ethoxy-5-(2-methoxyethoxymethoxyphenyl)-2-cyclohexenoneHCID 20552111—
ReactantHCID 178506846HCID 178506846—
SolventBenzeneHCID 241—
Product3-Ethyl-5-(2-methoxyethoxymethoxyphenyl)-2-cyclohexenoneHCID 20552117—

Reaction Steps

A solution of 3-ethoxy-5-(2-methoxyethoxymethoxyphenyl)-2-cyclohexenone (2.0 g) in benzene (60 ml) was added dropwise with stirring in an atmosphere of dry nitrogen to an ice-cooled 1.5 M solution of ethyllithium in benzene (20.8 ml). When the addition was complete, water was added and the mixture was allowed to stand overnight at room temperature. The benzene layer was separated and the aqueous layer was extracted with ether. The organic solutions were combined, dried and the solvents were evaporated under reduced pressure. The residue was purified by preparative-layer chromatography on silica gel using a mixture of ethyl acetate and petroleum ether (b.p. 60°-80°) for elution to afford the title compound (0.65 g) as a pale yellow oil. (Found: C, 70.9; H, 7.7. C18H24O4 requires C, 71.0; H, 7.9%.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04315006
Source datasetuspto-grants-1982_02
ORD IDord-c5fe46a367fe4ec0b1f2824a37ea6ece
Source noteuspto-grants-1982_02