HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → Methyl 2-oxo-5-(pyridin-4-yl)cyclohexane-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 53880921 | HCID 53880921 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 2-oxo-5-(pyridin-4-yl)cyclohexane-1-carboxylate | HCID 13986053 | 39.8% |
Reaction Steps
To 100 ml of tetrahydrofuran, there was added 13 g of potassium t-butoxide. A solution of 26 g of 4-(4-pyridyl)pimelic acid methyl ester in 50 ml of tetrahydrofuran was added at 20° to 40° C. and the mixture was stirred for 2 hours. After the reaction was completed, the mixture was treated with saturated aqueous solution of ammonium chloride and then extracted with ether. The ether solution was washed with water and dried. Ether was distilled off and the residue was recrystallized from ether. There was obtained 9.6 g of 2-methoxycarbonyl-4-(4-pyridyl)cyclohexanone: m.p. 82°-83° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05047545 |
| Source dataset | uspto-grants-1991_09 |
| ORD ID | ord-544212aabfe7409a911fa91d30ca9b96 |
| Source note | uspto-grants-1991_09 |