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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 250827Generated: October 25, 2026

Trifluoromethanesulfonic anhydride → Methyl 3-(3'-methylaminobiphenyl-4-yl)propanoate

https://huagongshe.com/reaction/250827

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantBenzenepropanoic acid, 4-hydroxy-, methyl esterHCID 79706—
ReactantSodium BicarbonateHCID 516892—
Reactant[3-(Methylamino)phenyl]boronic acidHCID 23558980—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
SolventPotassium Phosphate, TribasicHCID 62657—
ProductMethyl 3-(3'-methylaminobiphenyl-4-yl)propanoateHCID 6727343362.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

1.0 g (5.5 mmol, 1.0 eq) of methyl 3-(4-hydroxyphenyl)propanoate is dissolved in 8 mL of dichloromethane in the presence of 1 ml of triethylamine. 1.12 mL (6.6 mmol, 1.2 eq) of triflic anhydride are added at 0° C. The reaction mixture is stirred for 1 hour at 0° C. The reaction is stopped by addition of 50 mL of saturated sodium hydrogen carbonate solution and then extracted with ethyl acetate. The organic phases are combined and dried over sodium sulfate. The solvents are evaporated off and the residue is then filtered on silica gel (1/1 heptane/ethyl acetate). After evaporating off the solvents, the oil obtained is dissolved in 6 mL of an 8/2 mixture of dimethylformamide and of 2M potassium phosphate solution. 1.0 g (6.6 mmol, 1.2 eq) of N-methyl-3-aminophenylboronic acid are added, along with 317 mg of tetrakis(triphenylphosphine)palladium. The reaction mixture is stirred for 3 hours at 90° C. The reaction is stopped by addition of 50 mL of water and then extracted with ethyl acetate. The organic phases are combined and dried over sodium sulfate. The solvents are evaporated off and the residue is then chromatographed on silica gel (70/30 heptane/ethyl acetate). 0.92 g of methyl 3-(3′-methylaminobiphenyl-4-yl)propanoate is obtained. Yield=61%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07863332B2
Source datasetuspto-grants-2011_01
ORD IDord-85a7627c56db48bbaeb41fb01e492ab4
Source noteuspto-grants-2011_01