HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 130707Erstellt: 25. Oktober 2026
Hydrochloric Acid → 2-(4-Methoxyphenyl)-2-methylpropanenitrile
https://huagongshe.com/reaction/130707
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Isobutyronitrile | HCID 6559 | — |
| Edukt | 4-Fluoroanisole | HCID 9987 | — |
| Edukt | Potassium bis(trimethylsilyl)amide | HCID 3251421 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 2-(4-Methoxyphenyl)-2-methylpropanenitrile | HCID 219166 | 52% |
Reaktionsschritte
Add potassium bis(trimethylsilyl)amide (39.90 g, 200 mmol) to a stirred solution of 4-fluoroanisole (15.0 mL, 133 mmol), isobutyronitrile (49.0 mL, 539 mmol) and anhydrous tetrahydrofuran (150 mL). Heat the reaction to reflux under nitrogen for 72 h. Cool the reaction to room temperature, pour it into 1 N hydrochloric acid (300 mL), and extract with diethyl ether (3×100 mL). Wash the diethyl ether extracts with brine (100 mL), dry the extracts over magnesium sulfate, filter, and concentrate on a rotary evaporator to give the crude product. The crude product is purified by flash chromatography on silica gel eluting with 10% ethyl acetate/hexanes to yield 12.13 g (52%) of 2-(4-methoxy-phenyl)-2-methyl-propionitrile: TLC: Rf in 10% ethyl acetate/hexanes: 0.30; 1H NMR (CDCl3): 7.40-7.37 (m, 2H), 6.92-6.90 (m, 2H), 3.81 (s, 3H), 1.70 (s, 6H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07381719B2 |
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| Quelldatensatz | uspto-grants-2008_06 |
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| ORD ID | ord-ccf243a42fc24f19b931160a3d67fead |
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| Quellennotiz | uspto-grants-2008_06 |
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