HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 593722Erstellt: 24. Oktober 2026
3-Bromo-2-fluorobenzaldehyde → (3-Bromo-2-fluorophenyl)(4-fluorophenyl)methanol
https://huagongshe.com/de/reaction/593722
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 3-Bromo-2-fluorobenzaldehyde | HCID 22019361 | — |
| Edukt | HCID 178418676 | HCID 178418676 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | (3-Bromo-2-fluorophenyl)(4-fluorophenyl)methanol | HCID 86730390 | — |
Reaktionsschritte
To a solution of 3-bromo-2-fluorobenzaldehyde (0.150 g, 0.739 mmol) in THF (3.21 mL) cooled to −78° C. was added (4-fluorophenyl)magnesium bromide (0.443 mL, 0.887 mmol). The reaction mixture was maintained at −78° C. for at least 1 hr, then allowed to warm to room temperature slowly over 2 hr. The reaction was quenched with a saturated aqueous solution of NH4Cl. The reaction mixture was diluted with CH2Cl2 and the layers were separated. The aqueous phase was extracted with CH2Cl2 (2×). Organics were combined, dried over Na2SO4, filtered, and concentrated to afford the title compound as a yellow residue.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09242967B2 |
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| Quelldatensatz | uspto-grants-2016_01 |
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| ORD ID | ord-c9632efbb6ef4d2c994b06af3aa332dc |
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| Quellennotiz | uspto-grants-2016_01 |
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