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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606508Generated: October 25, 2026

Toluene → methyl N-[(3'-cyanobiphenyl-4-yl)sulfonyl]valinate

https://huagongshe.com/reaction/606508

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium CarbonateHCID 10340—
Reactant3-Cyanophenylboronic acidHCID 2734325—
Reactantmethyl N-[(4-bromophenyl)sulfonyl]-L-valinateHCID 47337186—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Productmethyl N-[(3'-cyanobiphenyl-4-yl)sulfonyl]valinateHCID 6676916097%

Reaction Steps

A suspension of methyl N-[(4-bromophenyl)sulfonyl]valinate obtained in Reference Example 92 (5.00 g, 14.3 mmol), (3-cyanophenyl)boronic acid (2.52 g, 17.1 mmol), tetrakis(triphenylphosphine)palladium (0.330 g, 0.286 mmol) and 2N aqueous sodium carbonate solution (8.57 mL, 17.1 mmol) in EtOH (15 mL)-toluene (50 mL) was heated under reflux for 8 hr under nitrogen atmosphere. The reaction mixture was diluted with ethyl acetate, washed with water and saturated brine, and dried over sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was crystallized from hexane-ethyl acetate to give the title compound as a yellow powder (5.18 g, 97%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915267B2
Source datasetuspto-grants-2011_03
ORD IDord-8b03e056be9b4eecb0cb5a8f50d27b6a
Source noteuspto-grants-2011_03