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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Propylphosphonic anhydride | HCID 111923 | — |
| Reactant | 5-Bromo-2-methylbenzoic acid | HCID 346004 | — |
| Reactant | Methyl 3-amino-2,4-dimethylbenzoate | HCID 66871802 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 3-[(5-bromo-2-methyl-benzoyl)amino]-2,4-dimethyl-benzoate | HCID 86707319 | 88.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08933098B2 |
|---|
| Source dataset | uspto-grants-2015_01 |
|---|
| ORD ID | ord-f4c4e6538b6648feab4928a5c7796567 |
|---|
| Source note | uspto-grants-2015_01 |
|---|