HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 43319Generated: October 25, 2026
Hydrochloric Acid → HCID 91080937, compound
https://huagongshe.com/reaction/43319
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 5-(Tetrahydro-2H-pyran-4-YL)cyclohexane-1,3-dione | HCID 18921363 | — |
| Reactant | HCID 178476522 | HCID 178476522 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 91080937 | HCID 91080937 | — |
Reaction Steps
To a mixture of 5-(tetrahydropyran-4-yl)cyclohexane-1,3-dione (196 mg; 1 mmol) and 4-dimethylaminopyridine (610 mg; 5 mmol) is added dry chloroform (4 ml) under an atmosphere of nitrogen, and the mixture is stirred at room temperature until all the solids are dissolved. To this solution is then added dry toluene (2 ml) and a solution of 3,5-dimethylbiphen-4-yllead triacetate (1.2 mmol) in chloroform. The reaction mixture is heated under reflux for 1 hour. The reaction mixture is cooled to room temperature, acidified to pH 1 with 2N aqueous hydrochloric acid, filtered and the filtrate is extracted with dichloromethane (2×40 ml). The organic extracts are combined, dried over anhydrous magnesium sulfate, filtered and the filtrate is evaporated in vacuo. The residue is purified by column chromatography on silica gel to give 2-(3,5-dimethylbiphen-4-yl)-5-(tetrahydropyran-4-yl)cyclohexane-1,3-dione.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08536351B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-ab0ad6a964094714b12416aad178ce3c |
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| Source note | uspto-grants-2013_09 |
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