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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 418892Generated: October 25, 2026

Sodium ethoxide → 1-(3-Methoxyphenyl)-2-(ethoxycarbonylmethyl)cyclohexene

https://huagongshe.com/reaction/418892

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ethoxideHCID 2723922—
ReactantEthyl [2-(3-methoxyphenyl)-cyclohexylidene]acetateHCID 53720108—
SolventDimethyl SulfoxideHCID 679—
Product1-(3-Methoxyphenyl)-2-(ethoxycarbonylmethyl)cyclohexeneHCID 1935848892%

Reaction Conditions

Temperature100 °C

Reaction Steps

Combine [2-(3-methoxy-phenyl)-cyclohexylidene]-acetic acid ethyl ester (839.4 mg, 3.06 mmol), sodium ethoxide (62.5 mg, 0.92 mmol), and DMSO (6.0 mL), stir, and heat at 100° C. After 2 hours, cool to ambient temperature and extract the organic layer with ethyl acetate. Wash the ethyl acetate layer 5× with brine and dry the organic layer over sodium sulfate, and concentrate in vacuo to yield the titled compound (769.6 mg, 92%) as a clear oil. TLC Rf=0.58 in 8:1 hexanes:ethyl acetate. 1H NMR (CDCl3): 7.21 (m, 1H), 6.75 (m, 3H), 4.11 (q, 2H, J=7.2 Hz), 3.79 (s, 3H), 2.91 (s, 2H), 2.28 (m, 2H), 2.12 (m, 2H), 1.72 (m, 4H), 1.24 (t, 3H, J=7.3 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093302B2
Source datasetuspto-grants-2012_01
ORD IDord-6fb12fd57b0f47369b2c163c09bed044
Source noteuspto-grants-2012_01