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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 3-Ethoxy-5-(2-methoxyethoxymethoxyphenyl)-2-cyclohexenone | HCID 20552111 | — |
| Reactant | HCID 178506846 | HCID 178506846 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 3-Ethyl-5-(2-methoxyethoxymethoxyphenyl)-2-cyclohexenone | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04315006 |
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| Source dataset | uspto-grants-1982_02 |
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| ORD ID | ord-c5fe46a367fe4ec0b1f2824a37ea6ece |
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| Source note | uspto-grants-1982_02 |
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