HuagongsheHuagongshe Chemistry Print Report · For research reference only
m-Nitroacetophenone → 2-Chloro-1-(3-nitrophenyl)ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | m-Nitroacetophenone | HCID 8494 | — |
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Solvent | Diisopropyl Ether | HCID 7914 | — |
| Product | 2-Chloro-1-(3-nitrophenyl)ethanone | HCID 7437 | 83.2% |
Reaction Steps
3′-Nitroacetophenone (2.00 g) was dissolved in diisopropyl ether (12.1 ml) and sulfuryl chloride (6.70 g) was added all at once thereto at 22° C. and refluxed for 6.5 hours. The reaction mixture was allowed to cool to room temperature while stirring, and the precipitated solids were filtered and washed with diisopropyl ether. Drying under reduced pressure yielded the desired 2-chloro-3′-nitroacetophenone (2.01 g; 83.1%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06696573B1 |
| Source dataset | uspto-grants-2004_02 |
| ORD ID | ord-51086aa603e145a4ab2999cf686bed9a |
| Source note | uspto-grants-2004_02 |