HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → 2,2-Difluorocyclopropyl(4-chlorophenyl) ketone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2,2-difluoro-N-methoxy-N-methylcyclopropane-1-carboxamide | HCID 53416131 | — |
| Reactant | HCID 178419578 | HCID 178419578 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,2-Difluorocyclopropyl(4-chlorophenyl) ketone | HCID 24865871 | — |
Reaction Steps
A solution of 2.00 g (12.1 mmol) of the compound from Example 120A in 20 ml of THF was added under argon to 2.87 g (13.3 mmol) of a 1N chlorophenylmagnesium bromide solution in diethyl ether in 20 ml of THF at RT, and the mixture was heated under reflux for 2 h. The reaction mixture was added to saturated aqueous ammonium chloride solution and extracted twice with diethyl ether, and the combined organic phases were dried over magnesium sulfate and concentrated. 2.47 g (94% of theory) of the title compound were obtained and were reacted without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08063234B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-2dc7db6623e64040b431f836187bbf19 |
| Source note | uspto-grants-2011_11 |