HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 561420Erstellt: 26. Oktober 2026
Water → (4-Fluoro-2-methylphenyl)(4-fluorophenyl)methanol
https://huagongshe.com/reaction/561420
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | 4-Fluorobenzaldehyde | HCID 68023 | — |
| Edukt | 2-Bromo-5-fluorotoluene | HCID 96743 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Hexane | HCID 8058 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | (4-Fluoro-2-methylphenyl)(4-fluorophenyl)methanol | HCID 58392149 | — |
Reaktionsschritte
1.00 g (5.29 mmol) of 2-bromo-5-fluorotoluene were dissolved in 10 ml of tetrahydrofuran at −78° C. Addition of 4.0 ml (6.35 mmol) of a 1.6N solution of n-butyllithium in hexane was followed by stirring for 15 min, and then 0.79 g (6.35 mmol) of p-fluorobenzaldehyde dissolved in 10 ml of tetrahydrofuran was added dropwise. The mixture was warmed to RT and stirred for 1 h. The reaction solution was mixed with water and ethyl acetate, and the phases were separated. The aqueous phase was extracted three times with ethyl acetate, and the combined organic phases were washed with saturated aqueous sodium chloride solution. The solvents were removed in vacuo, and the crude product was purified by preparative HPLC (mobile phase: acetonitrile-water gradient). 0.56 g (43% of theory) of the title compound was obtained.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US08063234B2 |
|---|
| Quelldatensatz | uspto-grants-2011_11 |
|---|
| ORD ID | ord-72a9b7629bdb48c7b48f8b0ed345465d |
|---|
| Quellennotiz | uspto-grants-2011_11 |
|---|