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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1427087Generated: October 26, 2026

Diisopropylethylamine → Methyl 3-[(5-bromo-2-methyl-benzoyl)amino]-2,4-dimethyl-benzoate

https://huagongshe.com/reaction/1427087

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantPropylphosphonic anhydrideHCID 111923—
Reactant5-Bromo-2-methylbenzoic acidHCID 346004—
ReactantMethyl 3-amino-2,4-dimethylbenzoateHCID 66871802—
SolventDichloromethaneHCID 6344—
ProductMethyl 3-[(5-bromo-2-methyl-benzoyl)amino]-2,4-dimethyl-benzoateHCID 8670731988.6%

Reaction Steps

To a solution of 5-bromo-2-methylbenzoic acid (2.0 g, 0.0093 mol) in CH2Cl2 (20 mL) at 0° C. are added methyl 3-amino-2,4-dimethylbenzoate (1.49 g, 0.0084 mol, see preparation 10) and N,N-diisopropylethylamine (4.79 g, 0.0372 mol). After stirring the reaction mixture for 10 minutes, 1-propanephosphonic acid cyclic anhydride (50% solution in ethyl acetate, 8.87 g, 0.028 mol) is added via syringe and stirred at 50° C. After 16 hours, the solvent is removed under reduced pressure and the residue is diluted with water and extracted twice with ethyl acetate. The organic layers are combined and dried over anhydrous Na2SO4, filtered, and concentrated under reduced pressure. The resulting residue is purified by flash chromatography (silica gel) using 10% ethyl acetate in hexane to give the title compound as a white solid (2.80 g, 80%). Mass spectrum (m/z): 376.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933098B2
Source datasetuspto-grants-2015_01
ORD IDord-f4c4e6538b6648feab4928a5c7796567
Source noteuspto-grants-2015_01