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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383263Generated: November 1, 2026

4-Bromo-2-nitrophenol → 2-Amino-4-Bromophenol

https://huagongshe.com/reaction/383263

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-2-nitrophenolHCID 24364—
ReactantStannous ChlorideHCID 24479—
ReactantSodium BicarbonateHCID 516892—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product2-Amino-4-BromophenolHCID 35184089.2%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of compound 4-bromo-2-nitrophenol (1 g, 4.59 mmol) and SnCl2 (5.2 g, 22.9 mmol) in ethanol (10 mL) was stirred at 70° C. for 2 h. After cooled down, the mixture was diluted with water (100 mL), adjusted to pH 7 with saturated aqueous NaHCO3 and extracted with ethyl acetate (100 mL). The organic layer was washed with brine (50 mL), dried over Na2SO4, concentrated to give 2-amino-4-bromophenol (770 mg, 89%) as a grey solid. LCMS: 188 [M+1]+. 1H NMR (400 MHz, DMSO-d6) δ 4.79 (s, 2H), 6.48 (dd, J1=2.4 Hz, J2=8.4 Hz, 1H), 6.55 (d, J=8.4 Hz, 1H), 6.71 (d, J=2.4 Hz, 1H), 9.26 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367663B2
Source datasetuspto-grants-2013_02
ORD IDord-c38e6cc82a00442093a2e29ec3a8a771
Source noteuspto-grants-2013_02