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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSulfuric AcidHCID 1118—
Reactant2-Cyclopentyl-1-(2,3-dichloro-4-methoxyphenyl)ethanoneHCID 12395547—
Solvent1,4-DioxaneHCID 31275—
Product2-Cyclopentyl-1-(2,3-dichloro-4-methoxyphenyl)prop-2-en-1-oneHCID 1239555261.8%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04012524
Source datasetuspto-grants-1977_03
ORD IDord-cacf1411c85e46c9918ba4be1d295c53
Source noteuspto-grants-1977_03