HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 420329Erstellt: 25. Oktober 2026
Hydrochloric Acid → 5-tert-Butyl-2-fluoro-benzaldehyde
https://huagongshe.com/reaction/420329
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | Hexane | HCID 8058 | — |
| Edukt | 1-(1,1-Dimethylethyl)-4-fluorobenzene | HCID 136540 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 5-tert-Butyl-2-fluoro-benzaldehyde | HCID 59409516 | — |
Reaktionsschritte
A solution of 1-tert-butyl-4-fluoro-benzene (4.54 g, 30 mmol) in THF (100 mL) cooled at −78° C. was treated dropwise with a 2.5M solution of nBuLi in hexane (24 mL, 59 mmol). The reaction mixture was stirred for 5 h at −45° C. then DMF (3.5 mL, 44 mmol) was added at −75° C. and the reaction mixture was stirred for 0.5 h at −75° C. The reaction mixture was poured onto 1N aq. HCl and extracted with Et2O. Combined organic layers were washed with brine, dried over Na2SO4, filtered and evaporated. The title compound was obtained after chromatographic purification (Combi Flash, 40 g silica gel, hexane to hexane-EtOAc 10:1) as a light yellow oil: TLC (hexane-EtOAc 10:1) Rf=0.48, HPLC RtA=2.10 min; 1H NMR (400 MHz, CDCl3): δ10.36 (s, 1H), 7.85 (dd, 1H), 7.62 (m, 1H), 7.08 (dd, 1H), 1.32 (s, 9H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08093406B2 |
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| Quelldatensatz | uspto-grants-2012_01 |
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| ORD ID | ord-4272a5c506464c4e8293a5d378306f8b |
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| Quellennotiz | uspto-grants-2012_01 |
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