HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 30517Erstellt: 24. Oktober 2026
Isobutyric Acid → Allyl 1-{[(alpha-Isobutanoyloxyethoxy)carbonyl]aminomethyl}-1-Cyclohexane Acetate
https://huagongshe.com/de/reaction/30517
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Isobutyric Acid | HCID 6590 | — |
| Edukt | 4-Methylmorpholine | HCID 7972 | — |
| Edukt | Hexane | HCID 8058 | — |
| Edukt | Allyl 1-{[(alpha-Chloroethoxy)carbonyl]aminomethyl}-1-Cyclohexane Acetate | HCID 9995975 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | Allyl 1-{[(alpha-Isobutanoyloxyethoxy)carbonyl]aminomethyl}-1-Cyclohexane Acetate | HCID 9999163 | — |
Reaktionsschritte
A solution of compound (14) (38 g, 0.12 mol) in isobutyric acid (55 mL, 52.5 g, 0.6 mol) was added to a mixture of isobutyric acid (55 mL, 52.5 g, 0.6 mol) in N-methylmorpholine (65 mL, 60 g, 0.59 mol) at 0° C. over a period of 30 min. The resulting turbid solution was stirred for 16 h at room temperature. The reaction mixture was diluted with diethyl ether (500 mL) and washed with water (3×200 mL) followed by 10% potassium bicarbonate (4×200 mL) and brine (200 mL). The organic phase was dried over anhydrous sodium sulfate and concentrated to yield a viscous liquid. This crude product was purified by column chromatography on silica gel, eluting with 7.5% ethyl acetate:hexane to give the desired compound (15) as a clear, viscous liquid (37 g, 84% yield). 1H NMR (CDCl3, 400 MHz): δ 1.15 (d, 6H), 1.35-1.58 (m, 10H), 2.31 (s, 2H), 2.51 (m, 1H), 3.19 (d, 2H), 4.56 (d, 2H), 5.24 (dd, 1H), 5.32 (dd, 1H), 5.35 (br. s, 1H), 5.84-5.94 (m, 1H), 6.78 (q, 1H). MS (ESI) m/z 392.24 (M+H+).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07423169B2 |
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| Quelldatensatz | uspto-grants-2008_09 |
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| ORD ID | ord-4fe61ca5b772457c8464fb77c4ff4df2 |
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| Quellennotiz | uspto-grants-2008_09 |
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