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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1009222Generated: November 1, 2026

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

https://huagongshe.com/reaction/1009222

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-(cyclopropylmethoxy)propanoateHCID 67304435—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
Productmethyl (S)-2-cyclopropylmethoxy-3-[3'-(methylamino)biphenyl-4-yl]propanoateHCID 6730461345%

Reaction Conditions

Temperature90 °C

Reaction Steps

53 mg (0.046 mmol) of tetrakis(triphenylphosphine)palladium are added to a solution of 145 mg (0.46 mmol) of methyl (S)-3-(4-bromophenyl)-2-(cyclopropylmethoxy)propionate and 129 mg (0.55 mmol) of methyl[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]amine in 3 ml of dimethylformamide. 0.3 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). 70 mg of methyl (S)-2-cyclopropylmethoxy-3-[3′-(methylamino)biphenyl-4-yl]propanoate are obtained in the form of an oil. Yield=45%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973063B2
Source datasetuspto-grants-2011_07
ORD IDord-cfbcca531459448da90bca1d35b9367b
Source noteuspto-grants-2011_07