Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 887747Generated: October 25, 2026

3-Acetylamino-6-bromo-2-nitro-benzoic acid → Methyl 3-acetylamino-6-bromo-2-nitrobenzoate

https://huagongshe.com/reaction/887747

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Acetylamino-6-bromo-2-nitro-benzoic acidHCID 11403903—
Reactanttrimethylsilyldiazomethane Et2OHCID 23159941—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 3-acetylamino-6-bromo-2-nitrobenzoateHCID 1115125566.4%

Reaction Steps

To a mixed solution of 3-(acetylamino)-6-bromo-2-nitrobenzoic acid (2.00 g, 6.60 mmol) in methanol (20 mL) and tetrahydrofuran (5 mL) was added 2M trimethylsilyldiazomethane/diethyl ether solution (10.6 mL, 21.1 mmol) under ice-cooling, and the mixture was stirred at room temperature for 5 days. The reaction solution was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/hexane=25/75→60/40) to give the title compound (1.39 g, yield 66%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247429B2
Source datasetuspto-grants-2012_08
ORD IDord-ab75b8843663424d92e2efdb870c0921
Source noteuspto-grants-2012_08