HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 3-oxocyclohexanecarboxylate → HCID 178517489, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 3-oxocyclohexanecarboxylate | HCID 118096 | — |
| Reactant | 4-Chlorobenzene-1-carboximidamide hydrochloride | HCID 203436 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178517489 | HCID 178517489 | — |
Reaction Steps
7.5 g of ethyl 2-oxocyclohexane-4-carboxylate and 9.6 g of 4-chlorobenzamidine hydrochloride were introduced into 50 ml of methanol. 5.6 g of potassium tert-butylate were added with stirring. The reaction mixture was stirred under reflux for 4 hours and then poured onto ice water. The crystalline product was filtered off with suction, washed with water and recrystallized from dimethylformamide. Yield: 8.8 g; m.p.: >300° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06660746B1 |
| Source dataset | uspto-grants-2003_12 |
| ORD ID | ord-9f7b8dc8f11544988ea9ecdbbc059878 |
| Source note | uspto-grants-2003_12 |