HuagongsheHuagongshe Chemistry Print Report · For research reference only
(4-Chloro-3-(trifluoromethyl)phenoxy)benzaldehyde → 1-Chloro-2-(trifluoromethyl)-4-(4-vinylphenoxy)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (4-Chloro-3-(trifluoromethyl)phenoxy)benzaldehyde | HCID 86676377 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Catalyst | Methyltriphenyliphosphonium bromide | HCID 74505 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Chloro-2-(trifluoromethyl)-4-(4-vinylphenoxy)benzene | HCID 66825837 | 74.2% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a suspension of methyl(triphenyl)phosphonium bromide (5.56 g, 15.57 mmol) in anhydrous tetrahydrofuran (THF) (50 mL) was added BuLi (9.5 ml, 15.20 mmol) dropwise at 0° C. The reaction mixture was turned to clear and stirred for 15 min at 0° C., then a solution of -{[4-chloro-3-(trifluoromethyl)phenyl]oxy}benzaldehyde (4.07 g, 13.54 mmol) in THF (10 mL) was added. The reaction mixture was warmed to rt and stirred for 1 h, quenched by sat. NH4Cl, and then concentrated. The residue was dissolved in ethyl acetate (100 mL), washed with water, and brine, dried over anhydrous sodium sulfate, concentrated. Purification via ISCO afforded the title compound (3.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08975400B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-c07d1c13a6c84b7385b89a4e3d4b19a6 |
| Source note | uspto-grants-2015_03 |