HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitroethane → HCID 178446908, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitroethane | HCID 6587 | — |
| Reactant | Benzyltrimethylammonium hydroxide | HCID 66854 | — |
| Reactant | HCID 178458219 | HCID 178458219 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178446908 | HCID 178446908 | 19.2% |
Reaction Steps
Nitroethane (3g; 40 m mole) in ethanol (120 ml) was heated under reflux and under nitrogen for 10 minutes with benzyltrimethyl ammonium hydroxide (1 ml) and then cooled to room temperature. Acryloylferrocene (6.5g; 27.1 mole) was then added and the solution was stirred for 1 hour and then filtered. The filtrate was concentrated on the rotary evaporator, then poured into water and extracted with chloroform. The organic extract was washed (water) and dried (sodium sulphate) to give a brown solid which was recrystallised from cyclohexane/petroleum ether to give 4-nitropentanoyl ferrocene (1.65g; 19.2%) mp 79°-80°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03966783 |
| Source dataset | uspto-grants-1976_06 |
| ORD ID | ord-2d33208e1b9e48c7ab59e730dedcdacd |
| Source note | uspto-grants-1976_06 |