HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1865449Generated: October 31, 2026
Water → methyl (S)-2-propyloxy-3-[3'-(methylamino)biphenyl-4-yl]propanoate
https://huagongshe.com/reaction/1865449
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | N-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline | HCID 57976762 | — |
| Reactant | methyl (S)-3-(4-bromophenyl)-2-(propyloxy)propanoate | HCID 67305005 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | methyl (S)-2-propyloxy-3-[3'-(methylamino)biphenyl-4-yl]propanoate | HCID 67305428 | 70.3% |
Reaction Steps
38 mg (0.033 mmol) of tetrakis(triphenylphosphine)palladium are added to a solution of 100 mg (0.33 mmol) of methyl (S)-3-(4-bromophenyl)-2-(propyloxy)propionate and 90 mg (0.39 mmol) of methyl[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]amine in 1 ml of dimethylformamide. 0.2 ml of a 2M potassium phosphate solution is added and the reaction mixture is stirred at 90° C. for 2 hours. The reaction is halted by the addition of 10 ml of water and then extraction is carried out with ethyl acetate. The organic phases are combined and dried over sodium sulfate. The solvents are evaporated and then the residue is chromatographed on silica gel (heptane/ethyl acetate 80/20). 76 mg of methyl (S)-2-propyloxy-3-[3′-(methylamino)biphenyl-4-yl]propanoate are obtained in the form of an oil. Yield=70%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07626054B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-fdddbb17d11847068ff2573a8ab7ed49 |
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| Source note | uspto-grants-2009_12 |
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