HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 624349Generated: October 31, 2026
Dimethylformamide → 2-chloro-4,4-diMethylcyclohex-1-enecarbaldehyde
https://huagongshe.com/reaction/624349
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Cyclohexanone, 3,3-dimethyl- | HCID 76322 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-chloro-4,4-diMethylcyclohex-1-enecarbaldehyde | HCID 86642872 | — |
Reaction Steps
Into a 250 mL round-bottomed flask was added N,N-dimethylformamide (3.5 mL) in dichloromethane (30 mL) to give a colorless solution. The mixture was cooled to −10° C., and phosphoryl trichloride (4 mL) was added dropwise. The solution was warmed up to room temperature, and 3,3-dimethylcyclohexanone (5.5 mL) was added slowly. The mixture was heated to reflux for overnight. The reaction mixture was quenched by 0° C. solution of sodium acetate (25 g in 50 mL water). The aqueous layer was extracted with ether (3×200 mL). The organic layers were combined, dried over Na2SO4, filtered, and dried under vacuum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09303025B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-c7c7396e89e347b09c858efba65bd40f |
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| Source note | uspto-grants-2016_04 |
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