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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1778404Generated: October 31, 2026

Acetic Acid → Methyl 2,6-diamino-3-bromobenzoate

https://huagongshe.com/reaction/1778404

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantFormic AcidHCID 284—
ReactantEthanolHCID 702—
ReactantMethyl 6-amino-3-bromo-2-nitrobenzoateHCID 66685320—
CatalystIronHCID 23925—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductMethyl 2,6-diamino-3-bromobenzoateHCID 6668563275.2%

Reaction Steps

Iron powder (4.07 g) was added slowly with stirring and cooling to a solution of methyl 6-amino-3-bromo-2-nitrobenzoate (prepared according to Brock et al, Tetrahedron, 1963, 19, 1911, 2.0 g) in a mixture of absolute ethanol (49 mL), acetic acid (5 mL), formic acid (0.7 mL) and water (15 mL). On completion of the addition, the mixture was stirred at room temperature for 2 hours. The mixture was diluted with DCM and water (1:1) then filtered through Celite. The layers were separated and the aqueous layer was extracted with DCM. The combined organic layers were washed with 1M aqueous sodium hydroxide solution, dried (MgSO4) and filtered. The filtrate was evaporated to dryness and the residue was triturated with ether and cyclohexane (1:1) and the solid was collected by filtration to give methyl 3-bromo-2,6-diaminobenzoate (1.34 g) as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266896B2
Source datasetuspto-grants-2016_02
ORD IDord-9ef6d389d16d47509fc4b05d4d801cf4
Source noteuspto-grants-2016_02