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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7769Generated: October 25, 2026

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

https://huagongshe.com/reaction/7769

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-2-nitrophenolHCID 24364—
ReactantStannous chloride dihydrateHCID 61436—
ReactantSodium BicarbonateHCID 516892—
SolventMethanolHCID 887—
Product2-Amino-4-BromophenolHCID 351840—

Reaction Steps

To a stirred solution of 4-bromo-2-nitrophenol (5.00 g, 22.9 mmol) in MeOH (120 mL) was added tin(II) chloride dihydrate (15.53 g, 68.8 mmol). The reaction mixture was heated at reflux and monitored by LC/MS. When significant reduction was complete, the reaction mixture was cooled to rt, poured over ice, and made basic (pH 9) with 50% saturated NaHCO3. The aqueous layer was extracted with EtOAc (2×150 mL) and the combined extracts washed with brine, dried over MgSO4, filtered, and concentrated in vacuo to give 2-amino-4-bromophenol as a dark gray solid. 1H NMR (CDCl3, 300 MHz) δ 9.29 (br s, 1H), 6.71 (d, 1H), 6.56 (d, 1H), 6.49 (dd, 1H), 4.83 (br s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07087601B2
Source datasetuspto-grants-2006_08
ORD IDord-c8eb1ab15de24a91a8d47e2209a31578
Source noteuspto-grants-2006_08