HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 257604Generated: October 30, 2026
1-Chloro-4-(chloromethyl)benzene → HCID 11076339, compound
https://huagongshe.com/reaction/257604
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Chloro-4-(chloromethyl)benzene | HCID 7723 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Dimedone | HCID 31358 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 11076339 | HCID 11076339 | 42% |
Reaction Steps
449 g (3.21 mols) dimedone (5,5-dimethylcyclohexane-1,3-dione) were added to a solution of aqueous potassium hydroxide comprising 166 g of 85% potassium hydroxide (2.52 mols) in 700 ml of water. The mixture was then warmed and a clear orange solution was obtained at 47° C. The solution was then heated to 59° C. and 544 g (3.21 mols) molten 4-chlorobenzyl chloride were added over a period of 1 hour with further heating to 85° C. Heating was continued for a further 2.5 to 3 hours up to a temperature of 100° C. The mixture was then cooled, the solid product filtered off, washed with water and dried in a vacuum oven at 50° C. The crude solid (815 g) was then dissolved in 2,400 ml methanol at reflux and 200 ml water added to produce a permanent cloudiness. The mixture was then allowed to cool to room temperature overnight with stirring. The solid so obtained was filtered, washed with about 400 ml cold methanol and dried in a vacuum oven to produce 340 g 2-(4-chlorobenzyl)-5,5-dimethylcyclohexane-1,3-dione as a white solid, m.pt. 188°-190° C. Yield: 42%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05262543 |
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| Source dataset | uspto-grants-1993_11 |
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| ORD ID | ord-6fb1466f1fec4b78ae1ec3d1149214dd |
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| Source note | uspto-grants-1993_11 |
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