HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2193011Erstellt: 27. Oktober 2026
Tris(hydroxymethyl)aminomethane → Tert-butyl 2-methylbutanoate
https://huagongshe.com/reaction/2193011
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Tris(hydroxymethyl)aminomethane | HCID 6503 | — |
| Edukt | 2-Methylbutanoic Acid | HCID 8314 | — |
| Edukt | Potassium tert-butoxide | HCID 23665647 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | Tert-butyl 2-methylbutanoate | HCID 523483 | — |
Reaktionsschritte
To a stirred solution of 2-methylbutanoic acid (1.029 Ml, 8.29 mmol) in DCM (10 Ml) was added potassium tert-butoxide (20 wt % in THF) (4.66 Ml, 8.29 mmol) dropwise at 0° C. The resulting suspension was allowed to warm to room temperature, and stirred for 1.5 hr. The reaction mixture was diluted with DCM (10 Ml), MP-®Trisamine Resin (3.86 g, 3.22 mMol/g; Argonaut Technologies, Inc.) was added, and the resulting suspension was stirred at room temperature for 1.5 hours. The resin was removed by vacuum filtration, and the resulting filtrate was washed with 1 N NaOH (1×20 Ml). The organic layer was dried over magnesium sulfate, filtered, and concentrated to afford tert-butyl 2-methylbutanoate. 1H NMR (500 MHz, CDCl3) δ 2.24 (sextet, 1H), 1.61 (m, 1H), 1.44-1.39 (overlapping s, m, 10H), 1.09 (d, 3H), 0.90 (t, 3H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08329722B2 |
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| Quelldatensatz | uspto-grants-2012_12 |
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| ORD ID | ord-dca8fe0f0dc64c51a32c3697e7d08d51 |
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| Quellennotiz | uspto-grants-2012_12 |
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