HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 596993Generated: October 28, 2026
Formaldehyde → 2-Cyclopentyl-1-(2,3-dichloro-4-methoxyphenyl)prop-2-en-1-one
https://huagongshe.com/reaction/596993
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 2-Cyclopentyl-1-(2,3-dichloro-4-methoxyphenyl)ethanone | HCID 12395547 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-Cyclopentyl-1-(2,3-dichloro-4-methoxyphenyl)prop-2-en-1-one | HCID 12395552 | 61.8% |
Reaction Steps
2',3'-Dichloro-4'-methoxy-2-cyclopentylacetophenone (51.6 g., 0.18 mole) is dissolved in dioxane (460 ml.) and paraformaldehyde (21.6 g., 0.72 mole) and concentrated sulfuric acid (9.65 g.) are added. The mixture is heated at 80°-85° C. for 20 hours. The dioxane is evaporated at reduced pressure. Water is added to the residual gum which then is extracted into ether. The ether extract is washed with water and dried over magnesium sulfate. The ether is evaporated and upon triturating the residue with hexane (5 ml.) there is obtained a solid that is crystallized from ligroin to obtain 2',3'-dichloro-4'-methoxy-2-cyclopentylacrylophenone (33.3 g.), m.p. 59°-63° C. Crystallization from butyl chloride affords a sample (m.p. 66°-67.5° C.) for analysis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04012524 |
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| Source dataset | uspto-grants-1977_03 |
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| ORD ID | ord-cacf1411c85e46c9918ba4be1d295c53 |
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| Source note | uspto-grants-1977_03 |
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