HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 2-Nitro-4-(trifluoromethyl)benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-Nitro-4-(trifluoromethyl)benzoyl chloride | HCID 14323524 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-Nitro-4-(trifluoromethyl)benzaldehyde | HCID 11160305 | 85.5% |
Reaction Steps
A mixture of 2-nitro-4-trifluoromethylbenzoyl chloride (8.0 g) and triphenylphosphine (16.5 g) in dry acetone (75 ml) was treated with bis-(triphenylphosphine)tetrahydroboratocopper(I) (19.8 g). The resulting suspension was stirred for 1 hour, filtered and washed with diethyl ether. The filtrate was evaporated to dryness and the resulting residue was subjected to chromatography, eluting with a mixture of diethyl ether and n-hexane (1:5 v/v), to give 2-nitro-4-trifluoromethylbenzaldehyde (5.91 g) in the form of an off-white solid, m.p. 63° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05650533 |
| Source dataset | uspto-grants-1997_07 |
| ORD ID | ord-645f1725a9424f278b6ce2bd0585fecb |
| Source note | uspto-grants-1997_07 |