Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Propargyl bromide | HCID 7842 | — |
| Edukt | Lithium diisopropylamide | HCID 2724682 | — |
| Edukt | 1-Tert-butyl 3-methyl pyrrolidine-1,3-dicarboxylate | HCID 4572775 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | HCID 57686375 | HCID 57686375 | 40,5% |
Reaktionsschritte
Pyrrolidine-1,3-dicarboxylic acid 1-tert-butyl ester 3-methyl ester 1 (6 mmol) was dissolved in THF (20 mL) and cooled down to −78° C. in a dry ice-acetone bath. LDA (5 mL, 2.0 M, 10 mmol) was then added dropwise. The mixture was stirred at −78° C. for 1 hr. Propargyl bromide (1.5 mL) was added in neat. The reaction was allowed to warm to rt naturally and stirred for 24 hrs. It was then quenched with sat. NH4Cl solution, extracted with ethyl acetate 2×50 mL. The organic layer was washed with brine, dried (MgSO4) and concentrated. The crude was purified on silica gel column using 4:1 hexanes/ethyl acetate to get the title compound (0.65 g) as an off-white gum. MS (267, M+H)
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08546404B2 |
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| Quelldatensatz | uspto-grants-2013_10 |
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| ORD ID | ord-958c55e717914987b3bb92a34f02a820 |
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| Quellennotiz | uspto-grants-2013_10 |
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