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HRID 81340Erstellt: 24. Oktober 2026

[4-(4-Cyanophenyl)but-3-ynyl]carbamic acid tert-butyl ester → [4-(4-Cyanophenyl)butyl]carbamic acid tert-butyl ester

https://huagongshe.com/de/reaction/81340

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt[4-(4-Cyanophenyl)but-3-ynyl]carbamic acid tert-butyl esterHCID 67364707—
EduktHCID 178418361HCID 178418361—
KatalysatorPalladiumHCID 23938—
LösungsmittelEthanolHCID 702—
Produkt[4-(4-Cyanophenyl)butyl]carbamic acid tert-butyl esterHCID 6736607987,3%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08846688B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-8dac3a66badc4fa2b709fec25abc6ec0
Quellennotizuspto-grants-2014_09