HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
[4-(4-Cyanophenyl)but-3-ynyl]carbamic acid tert-butyl ester → [4-(4-Cyanophenyl)butyl]carbamic acid tert-butyl ester
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | [4-(4-Cyanophenyl)but-3-ynyl]carbamic acid tert-butyl ester | HCID 67364707 | — |
| Edukt | HCID 178418361 | HCID 178418361 | — |
| Katalysator | Palladium | HCID 23938 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | [4-(4-Cyanophenyl)butyl]carbamic acid tert-butyl ester | HCID 67366079 | 87,3% |
Reaktionsschritte
A suspension of [4-(4-cyanophenyl)but-3-ynyl]carbamic acid tert-butyl ester 56 (5.2 g, 19.2 mmol) and 10% palladium on carbon (2.5 g, wet) in ethanol/THE (30 mL, 1:1) was stirred overnight under 1 atmosphere of hydrogen. After purging with nitrogen, the reaction mixture was suction filtered through a pad of Celite. The solvent was removed from the filtrate by evaporation. The residue was chromatographed on silica gel, eluting with methylene chloride/ethyl acetate (30:1), to afford the pure product 57 (4.6 g, 87%) as an oil. 1H NMR (300 MHz, CDCl3) δ 1.44 (s, 9H), 1.51 (m, 2H), 1.65 (m, 2H), 2.69 (t, 2H), 3.14 (m, 2H), 4.52 (br s, 1H), 7.27 (d, 2H), 7.56 (d, 2H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08846688B2 |
| Quelldatensatz | uspto-grants-2014_09 |
| ORD ID | ord-8dac3a66badc4fa2b709fec25abc6ec0 |
| Quellennotiz | uspto-grants-2014_09 |