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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1865451Generated: October 30, 2026

Water → methyl (S)-2-benzyloxy-3-[3'-(methylamino)biphenyl-4-yl]propanoate

https://huagongshe.com/reaction/1865451

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantN-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)anilineHCID 57976762—
Reactantmethyl (S)-3-(4-bromophenyl)-2-benzyloxypropanoateHCID 67304959—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
Productmethyl (S)-2-benzyloxy-3-[3'-(methylamino)biphenyl-4-yl]propanoateHCID 6730567263%

Reaction Conditions

Temperature70 °C

Reaction Steps

635 mg (0.55 mmol) of tetrakis(triphenylphosphine)palladium are added to a solution of 4 g (11 mmol) of methyl (S)-3-(4-bromophenyl)-2-benzyloxypropionate and 4 g (17 mmol) of methyl[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]amine in 25 ml of dimethylformamide. 10 ml of a 2M potassium phosphate solution are added and the reaction mixture is stirred at 70° C. for 1 hour. The reaction is halted by the addition of 50 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). 2.6 g of methyl (S)-2-benzyloxy-3-[3′-(methylamino)biphenyl-4-yl]propanoate are obtained in the form of an oil. Yield=61%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07626054B2
Source datasetuspto-grants-2009_12
ORD IDord-092dd148eec84bee83eea0a2d8162b40
Source noteuspto-grants-2009_12