HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1084655Generated: October 26, 2026
Hydrochloric Acid → 2-(2,4-Dichlorobenzoyl)-4,4-dimethylcyclohexane-1,3-dione
https://huagongshe.com/reaction/1084655
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,3-Cyclohexanedione, 4,4-dimethyl- | HCID 136360 | — |
| Reactant | 2,4-Dichlorobenzoyl Cyanide | HCID 9834232 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(2,4-Dichlorobenzoyl)-4,4-dimethylcyclohexane-1,3-dione | HCID 14749575 | 40% |
Reaction Steps
4,4-Dimethyl-1,3-cyclohexanedione [14.0 grams (g), 0.1 mole], 20.0 g (0.1 mole) 2,4-dichlorobenzoyl cyanide and 13.6 g (0.11 mole) anhydrous, powdered zinc chloride were combined in 100 milliliters (ml) methylene chloride. Triethylamine (10.1 g, 0.12 mole) was slowly added with cooling. The reaction mixture was stirred at room temperature for 5 hours and then poured into 2N hydrochloric acid. The aqueous phase was discarded and the organic phase was washed with 150 ml 5% Na2CO3 four times. The aqueous washings were combined and acidified with HCl, extracted with methylene chloride, dried and concentrated to yield 25.3 g of crude product. The crude product was chromatographed (2% AcOH/CH2Cl2) in 5 g aliquots then reduced on rotavap under reduced pressure at 50° C. for 30 minutes to remove AcOH. This yielded an oil (40% yield). The structure was confirmed by instrumental analysis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05006158 |
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| Source dataset | uspto-grants-1991_04 |
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| ORD ID | ord-732deb838f3a45578e51d4b5669985f4 |
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| Source note | uspto-grants-1991_04 |
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