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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Ethyl [2-(3-methoxyphenyl)-cyclohexylidene]acetate | HCID 53720108 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 1-(3-Methoxyphenyl)-2-(ethoxycarbonylmethyl)cyclohexene | HCID 19358488 | 92% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08093302B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-6fb12fd57b0f47369b2c163c09bed044 |
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| Source note | uspto-grants-2012_01 |
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