HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1501208Erstellt: 27. Oktober 2026
4-Bromo-3-fluorobenzaldehyde → 1-(4-Bromo-3-fluorophenyl)ethan-1-ol
https://huagongshe.com/reaction/1501208
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 4-Bromo-3-fluorobenzaldehyde | HCID 2783411 | — |
| Edukt | HCID 178418573 | HCID 178418573 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 1-(4-Bromo-3-fluorophenyl)ethan-1-ol | HCID 71756542 | — |
Reaktionsschritte
To a solution of 4-bromo-3-fluorobenzaldehyde (5 g, 24.75 mmol) in anhydrous tetrahydrofuran (100 mL) was added methyl magnesium bromide (3 M solution in tetrahydrofuran, 8.21 mL) at −45° C. under the atmosphere of nitrogen then stirred at room temperature. After 2 hours, LC-MS showed the desired product has received. The aqueous of ammonium chloride (15 mL) was added to quench the reaction, and extracted with ethyl acetate (50 mL), combined and concentrated the organic layers. The crude product was purified by column chromatography (petroleum ether/ethyl acetate=1:1) to give 1-(4-bromo-3-fluorophenyl)ethanol (4 g, 78%). LCMS (M+H+) m/z: calcd 217.97. found 218. 1H NMR (300 MHz, CD3OD): δ 7.92-7.87 (m, 1H), 7.23-7.19 (m, 1H), 7.07-7.10 (m, 1H), 4.80 (d, J=6.3 Hz, 1H), 1.41 (t, J=2.7 Hz, 3H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09206128B2 |
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| Quelldatensatz | uspto-grants-2015_12 |
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| ORD ID | ord-86254549ae6742c5aa12c4c86923c28f |
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| Quellennotiz | uspto-grants-2015_12 |
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