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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1784522Generated: October 30, 2026

Water → 2-Bromo-3,4-dimethylaniline

https://huagongshe.com/reaction/1784522

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantStannous chloride dihydrateHCID 61436—
ReactantSodium BicarbonateHCID 516892—
Reactant2-Bromo-3,4-dimethyl-1-nitrobenzeneHCID 825938—
SolventDimethylformamideHCID 6228—
Product2-Bromo-3,4-dimethylanilineHCID 66873106—

Reaction Steps

To a solution of 2-bromo-3,4-dimethylnitrobenzene (1.0 g, 4.35 mmole) in 10 mL DMF was added SnCl2.2H2O (4.92 g, 21.8 mmole). This solution was stirred overnight at room temperature 50 mL of H2O was added and the pH was adjusted to 8 with the addition of sat. NaHCO3 and extracted with 150 mL of EtOAC. The organic layer was dried over Na2SO4, filtered and evaporated yielding 2-bromo-3,4-dimethylaniline which was used as is in the conversion to 2-bromo-3,4-dimethyliodobenzene in a similar manner to that of Example 86. Compound 102 was prepared from 2-bromo-3,4-dimethyliodo-benzene using procedures similar to those of Examples 25 and 40. MS (ion spray): m/z 314.0/316.1 (M−H); 316.1/318.0 (M+H). 1H NMR: (DMSO-d6, 400 MHz) δ 7.37 (d, 1H), 7.15 (d, 1H), 2.43 (s, 3H), 2.37 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07504389B2
Source datasetuspto-grants-2009_03
ORD IDord-bacd7e94c6644747b69497e12a174d52
Source noteuspto-grants-2009_03