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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chloride | HCID 312 | — |
| Reactant | L-Phenylalanine | HCID 6140 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Iodobenzene | HCID 11575 | — |
| Catalyst | HCID 178424406 | HCID 178424406 | — |
| Solvent | N,N-Dimethylformamide--water (1/1) | HCID 21962138 | — |
| Product | 3-Phenyl-2-(phenylamino)propanoic acid | HCID 13416411 | 56% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08835682B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-09b285d5a4da49b981d1903a7bcfd70e |
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| Source note | uspto-grants-2014_09 |
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