HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1487025Erstellt: 26. Oktober 2026
Isobutylamine → 2,4-dimethyl-N-(2-methylpropyl)aniline
https://huagongshe.com/reaction/1487025
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Isobutylamine | HCID 6558 | — |
| Edukt | Tetrahydrofuran | HCID 8028 | — |
| Edukt | 1-Chloro-2,4-dimethylbenzene | HCID 523153 | — |
| Produkt | 2,4-dimethyl-N-(2-methylpropyl)aniline | HCID 28422389 | 96,3% |
Reaktionsschritte
A mixture of 1-chloro-2,4-dimethylbenzene (1687 mg, 12 mmol), isobutylamine (1755 mg, 24.00 mmol), and Caddick catalyst (140 mg, 0.238 mmol) was treated with lithium hexamethyl disilizide in tetrahydrofuran (1 M LHMDS in THF, 15 mL, 15.00 mmol) under nitrogen. The reaction mixture was heated to 70° C. for 45 minutes in a septum-sealed vessel. The cooled mixture was concentrated in vacuo and the residue was partitioned between aqueous citric acid (50 mL) and tert butyl methyl ether (TBME) (2×50 mL). The organic phase was treated with dried MgSO4, the solid removed by filtration and the organic phase was concentrated in vacuo to give (2,4-dimethylphenyl)(2-methylpropyl)amine (2.05 g, 11.56 mmol) as an orange oil. LCMS [LCMS1] Rt 1.03 min, m/z (ES+) 178 (M+H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09428452B2 |
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| Quelldatensatz | uspto-grants-2016_08 |
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| ORD ID | ord-c561e36556e34bc0ab77e7f6e38f36d6 |
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| Quellennotiz | uspto-grants-2016_08 |
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