HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → 6-Acetylamino-6-(2-chlorophenyl)-2-cyclohexen-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Dehydronorketamine | HCID 162835 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-Acetylamino-6-(2-chlorophenyl)-2-cyclohexen-1-one | HCID 20096600 | — |
Reaction Steps
Acetyl chloride (142 μl, 1.8 mmol) was added to a solution of 6-amino-6-(2-chlorophenyl)-2-cyclohexen-1-one (R. F. Parceli and J. P. Sanchez, J. Org. Chem., 46:5055 [1981]), (200 mg, 0.9 mmol) and triethylamine (1.0 ml) in dichloromethane (10 ml), and the reaction stirred at room temperature for 1 h. Analysis by TLC indicated complete reaction, and the mixture was partitioned between ethyl acetate and 1N HCI. The organic phase was washed with brine, dried (MgSO4), and the solvent removed by evaporation. Flash chromatography on silica gel eluted with 1:1 ethyl acetate/hexane afforded 6-acetylamino-6-(2-chlorophenyl)-2-cyclohexen-1-one which crystallized on standing, m.p. 144°-145° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05384331 |
| Source dataset | uspto-grants-1995_01 |
| ORD ID | ord-e38ed7566ec048d1830bf9515e619277 |
| Source note | uspto-grants-1995_01 |