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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217946Generated: October 25, 2026

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

https://huagongshe.com/reaction/217946

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[4-(4-Cyanophenyl)but-3-ynyl]carbamic acid tert-butyl esterHCID 67364707—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventTetrahydrofuran ethanolHCID 21873804—
Product[4-(4-Cyanophenyl)butyl]carbamic acid tert-butyl esterHCID 6736607987.3%

Reaction Steps

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/THF (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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198286B2
Source datasetuspto-grants-2012_06
ORD IDord-05b270af3eb4433e935d656b41e9d67d
Source noteuspto-grants-2012_06