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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2169122Generated: November 3, 2026

Sodium Carbonate → (2'-Chloro-biphenyl-2-yl)-acetonitrile

https://huagongshe.com/reaction/2169122

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantTriphenylphosphineHCID 11776—
Reactant2-Bromobenzyl cyanideHCID 29625—
Reactant2-Chlorophenylboronic acidHCID 2734322—
Catalystpalladium(II) acetateHCID 167845—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
Product(2'-Chloro-biphenyl-2-yl)-acetonitrileHCID 8672577884.4%

Reaction Steps

To a stirred solution of (2-bromophenyl)-acetonitrile (13) (5 g, 25.51 mmol) in a mixture of toluene and ethanol (1:1, 150 mL) was added 2-chloro phenyl boronic acid (14) (6 g, 38.2 mmol) and Na2CO3 (8.1 g, 76.53 mmol) at room temperature. Purging was conducting for 30 min with nitrogen. Then triphenyl phosphine (2.6 g, 10.2 mmol) was added followed by Pd(OAc)2 (0.287 g, 1.27 mmol) and further degassing was conducted for another 10 min. The reaction mixture was heated to reflux for 10 h. After completion of the reaction, the mixture was concentrated under reduced pressure to get a crude product which was purified using a silica column using 2% ethyl acetate in hexane to get (2′-chloro-biphenyl-2-yl)-acetonitrile (15) (4.9 g, 84.36%) as a yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045486B2
Source datasetuspto-grants-2015_06
ORD IDord-e960212be5be40c688cc65558aa7053d
Source noteuspto-grants-2015_06