HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → o-Nitrophenyl cyclopropyl ketone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Bromo-2'-nitrobutyrophenone | HCID 53773974 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | o-Nitrophenyl cyclopropyl ketone | HCID 10487947 | — |
Reaction Steps
A stirred mixture of 4-bromo-2'-nitrobutyrophenone (3.44 g, 0.013 mole) and NaOH (0.76 g, 0.019 mole) in water is heated at reflux temperature until reaction is complete by TLC, cooled to room temperature and extracted with diethyl ether. The ether extracts are combined, dried over Na2SO4 and concentrated in vacuo to give a dark brown liquid residue. The residue is taken up in diethyl ether, filtered through silica gel and concentrated in vacuo to give the title product as a yellow oil, identified by 1HNMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05364968 |
| Source dataset | uspto-grants-1994_11 |
| ORD ID | ord-0809fa1c0dc04d5da83ccd3896d794dd |
| Source note | uspto-grants-1994_11 |