HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dichloroethane → Benzyl 3-oxocyclohexanecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | 3-Oxocyclohexane-1-carboxylic acid | HCID 2760252 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Benzyl 3-oxocyclohexanecarboxylate | HCID 58964377 | — |
Reaction Steps
To a solution of 3-oxocyclohexane carboxylic acid (1.5 g, 10.6 mmol) in CH2Cl2 (35 mL) were added DMAP (0.129 g, 1.06 mmol), EDC (4.05 g, 21.1 mmol), and BnOH (1.2 mL, 11.6 mmol). The reaction was maintained at ambient temperature for 1 h. The reaction was further diluted with CH2Cl2, and then washed with saturated aqueous NaHCO3, followed by brine. The organic layer was separated, dried with MgSO4, filtered, and concentrated. The resulting crude product was used in the next step without further purification. LCMS: calculated for C14H16O3 232.28, observed m/e 233.1 (M+H)+ 255.0 (M+Na) (Rt 1.74/4 min).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08895596B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-600420e4e06b4ac9b8846904f3bc01a7 |
| Source note | uspto-grants-2014_11 |