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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284584Generated: October 28, 2026

Methyl iodide → Methyl 2-amino-5-bromo-3-methylbenzoate

https://huagongshe.com/reaction/2284584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantCesium carbonateHCID 10796—
Reactant2-Amino-5-bromo-3-methylbenzoic acidHCID 11850383—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductMethyl 2-amino-5-bromo-3-methylbenzoateHCID 276341389.1%

Reaction Steps

2-Amino-5-bromo-3-methylbenzoic acid (5.0 g, 21.7 mmol) in dry DMF (35 mL) was stirred with Cs2CO3 (10.62 g, 32.6 mmol) at room temperature for 1 h under nitrogen. Iodomethane (3.4 g, 1.5 mL, 23.95 mmol) in dry DMF (7 ml) was added dropwise to the above stirring reaction mixture over a period of 30 min and continued the reaction for 24 h. Reaction mixture was diluted with water (200 mL) and stirred to observe hetergeneous suspension. The purple solid was collected by filtration and dried to obtain methyl 2-amino-5-bromo-3-methylbenzoate (4.72 g, 89%). 1H NMR (DMSO-d6): δ 7.67 (app d, 1H, J=2.1 Hz), 7.34 (s, 1H), 6.60 (s, 2H), 3.78 (s, 3H), 2.09 (s, 3H).LCMS: rt 7.98 min (A), purity 99%, MS (m/e) 245 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145433B2
Source datasetuspto-grants-2015_09
ORD IDord-8048229c21674b33aba051b6813a27ee
Source noteuspto-grants-2015_09