Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diisopropylamine | HCID 7912 | — |
| Edukt | Tetrahydrofuran | HCID 8028 | — |
| Edukt | beta-nitrostyrene, (E)- | HCID 5284459 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Produkt | Lithium diisopropylamide | HCID 2724682 | — |
| Produkt | HCID 12709724 | HCID 12709724 | 84% |
Reaktionsschritte
An LDA (14 mmol) solution was prepared by treating diisopropylamine (1.37 g, 14 mmol) with BuLi (1.6 M, 8.5 mL, 14 mmol) at −78° C. in dry THF (10 mL) under argon and allowing to warm up to −20° C. This solution was then cooled to −60° C. added to a solution of 1-benzyl-piperidine-4-ethyl carboxylate (3.05 g, 12 mmol) in THF (8 mL) at −60° C. and allowed to warm up to −40° C. over 1 h whereupon a solution of trans-beta-nitrostyrene (1.93 g, 13 mmol) in THF (8 mL) was added dropwise. The reaction mixture was allowed to warm up to room temperature over 1 h and then quenched with ammonium chloride (saturated, 40 mL) and the product extracted with ethyl acetate (2×40 mL). The combined organic extracts were then washed with brine, dried over sodium sulfate, filtered and evaporated. Purification by chromatography on silica gel eluting with DCM:MeOH (9:1) afforded the title compound (4.1 g, 84%) as a light yellow gum. MS: m/e=397.4 (M+H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07173133B2 |
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| Quelldatensatz | uspto-grants-2007_02 |
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| ORD ID | ord-4cfcaf5e49ec43b695507a737ecaa876 |
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| Quellennotiz | uspto-grants-2007_02 |
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