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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1665728Generated: October 30, 2026

Potassium Carbonate → (4'-Cyano-biphenyl-3-yl)-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/1665728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Cyanophenylboronic acidHCID 2734326—
ReactantN-(tert-Butoxycarbonyl)-3-bromoanilineHCID 2757254—
CatalystHCID 178418397HCID 178418397—
SolventN,N-Dimethylformamide--water (1/1)HCID 21962138—
Product(4'-Cyano-biphenyl-3-yl)-carbamic acid tert-butyl esterHCID 6712068059%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 4-cyanobenzeneboronic acid (14.7 g, 0.10 mol), 3-bromo-phenyl-carbamic acid tert-butyl ester (27.2 g, 0.10 mol), Pd(Ph3P)4 (11.6 g, 0.01 mol) and K2CO3 (21 g, 0.15 mol) in DMF/H2O (1:1, 350 mL) was stirred under argon at 80° C. overnight. The DMF was evaporated under reduced pressure, and the residue was dissolved in EtOAc (200 mL). The mixture was washed with water and brine, dried over Na2SO4, and concentrated to dryness. The residue was purified by column chromatography (petroleum ether/EtOAc 50:1) on silica gel to give (4′-cyano-biphenyl-3-yl)-carbamic acid tert-butyl ester (17 g, 59%). 1H NMR (300 MHz, DMSO-d6) δ 9.48 (s, 1 H), 7.91 (d, J=8.4 Hz, 2 H), 7.85 (s, 1 H), 7.76 (d, J=8.4 Hz, 2 H), 7.32-7.48 (m, 3 H), 1.47 (s, 9 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08039491B2
Source datasetuspto-grants-2011_10
ORD IDord-394f163cd7c24dc4b02849d8554a856f
Source noteuspto-grants-2011_10