HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(Ethylthio)benzaldehyde → [2-(Benzyloxy)-5-(trifluoromethyl)phenyl][4-(ethylthio)phenyl]methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(Ethylthio)benzaldehyde | HCID 7006654 | — |
| Reactant | 1-(Benzyloxy)-2-bromo-4-(trifluoromethyl)benzene | HCID 18782669 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | [2-(Benzyloxy)-5-(trifluoromethyl)phenyl][4-(ethylthio)phenyl]methanol | HCID 86659305 | — |
Reaction Steps
A solution of butyl lithium (1.6M in hexane, 1.03 ml) was added to a stirred solution of the product from step (i) (0.5 g) in diethylether (20 ml) at −78° C. After 1 h, 4-ethylsulfanyl-benzaldehyde (0.25 g) was added and stirred for a further 1 h. The reaction was quenched with water, extracted with diethylether and the organic layer dried, then evaporated under reduced pressure. The residue was purified by chromatography on silica eluting with 50% diethylether/isohexane. Yield 0.7 g
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08003703B2 |
| Source dataset | uspto-grants-2011_08 |
| ORD ID | ord-a467342c61aa494aa924692feb8515fc |
| Source note | uspto-grants-2011_08 |