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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 600293Generated: October 29, 2026

Potassium Carbonate → (S)-tert-butyl 1-cyano-2-(3'-cyanobiphenyl-4-yl)ethylcarbamate

https://huagongshe.com/reaction/600293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3-Cyanophenylboronic acidHCID 2734325—
Reactant(S)-Tert-butyl (1-cyano-2-(4-iodophenyl)ethyl)carbamateHCID 57999650—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
SolventSodium chloride; waterHCID 57417360—
Product(S)-tert-butyl 1-cyano-2-(3'-cyanobiphenyl-4-yl)ethylcarbamateHCID 5799967290.2%

Reaction Conditions

Temperature75 °C

Reaction Steps

A solution of 3-cyanophenylboronic acid (4.74 g), (S)-tert-butyl 1-cyano-2-(4-iodophenyl)ethylcarbamate (10 g) and bis[bis(1,2-diphenylphosphino)-ethane]palladium (0) (0.243 g) in dioxane (100 mL) under nitrogen, was stirred for 10 min. A solution of potassium carbonate (7.43 g) in water (30 mL) was added and the resulting solution was stirred at 75° C. for 3 h. The cooled mixture was poured into water containing brine and extracted with ethyl acetate (3×150 mL). The combined organics were washed with saturated brine (3×50 mL), dried over sodium sulfate and adsorbed onto silica. The crude product was purified by flash silica chromatography, eluting with 20% ethyl acetate in isohexane. Pure fractions were evaporated to dryness to afford (S)-tert-butyl 1-cyano-2-(3′-cyanobiphenyl-4-yl)ethylcarbamate (8.42 g) as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902181B2
Source datasetuspto-grants-2011_03
ORD IDord-5e2ea4f11b1a492c822d78036c4699b7
Source noteuspto-grants-2011_03