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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 76972Generated: October 26, 2026

Chloride → 3-Phenyl-2-(phenylamino)propanoic acid

https://huagongshe.com/reaction/76972

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorideHCID 312—
ReactantL-PhenylalanineHCID 6140—
ReactantTriethylamineHCID 8471—
ReactantPotassium CarbonateHCID 11430—
ReactantIodobenzeneHCID 11575—
CatalystHCID 178424406HCID 178424406—
SolventN,N-Dimethylformamide--water (1/1)HCID 21962138—
Product3-Phenyl-2-(phenylamino)propanoic acidHCID 1341641156%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of (S)-2-amino-3-phenylpropanoic acid (1.52 g, 9.12 mmol) in a DMF/H2O mixture (10/1, 16.5 mL) maintained under nitrogen flowstream, iodobenzene (1.00 mL, 9.12 mmol), dichlorobis(tri-o-tolylphosphine)palladium(II) (357 mg, 0.42 mmol) CuI (86.4 mg, 0.42 mmol), K2CO3 (1.21 g, 9.12 mmol), rimethylbenzylammonium chloride (286 mg, 1.51 mmol) and triethylamine (TEA) (2.50 mL, 18.0 mmol) are added and the mixture stirred for 24 hours at 100° C. under nitrogen flowstream (LC-MS monitoring: complete conversion). The reaction mixture is partitioned between EtOAc and water; 1N HCl is added until pH=1 and the organic layer is separated, washed with brine and dried over Na2SO4. The resulting crude is purified by flash chromatography (DCM/MeOH=99/1) and 1.21 g of I21 is obtained (56% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835682B2
Source datasetuspto-grants-2014_09
ORD IDord-09b285d5a4da49b981d1903a7bcfd70e
Source noteuspto-grants-2014_09