HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4'-(Trifluoromethyl)-4-biphenylcarbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | n-Butyl lithium | HCID 61028 | — |
| Reactant | 4-Bromo-4'-(trifluoromethyl)biphenyl | HCID 12712349 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 4'-(Trifluoromethyl)-4-biphenylcarbaldehyde | HCID 2782712 | — |
Reaction Steps
N-Butyllitium in hexane (95 ml, 1.55M) was added dropwise to 4-Bromo-4'-trifluoromethylbiphenyl (40 g) in 250 ml of THF under N2 at -70° C. After addition the mixture was stirred for a further 10 mins and then dry dimethylformamide (19.49) in a solution of dry tetrahydrofuran (100 ml) was added dropwise. The mixture was then allowed to warm to room temperature in the absence of coolant. After stirring for 1.5 hours water was added and the mixture extracted with ether. The water washed and dried extracts were evaporated to give p-(4-trifluoromethylphenyl)benzaldehyde (34.5 g) m.p. 70°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04520007 |
| Source dataset | uspto-grants-1985_05 |
| ORD ID | ord-9d36cafe6e454d688a6364df5c155b1a |
| Source note | uspto-grants-1985_05 |