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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1786393Generated: October 31, 2026

2-Bromo-4-nitroanisole → 2-Bromo-4-nitrophenol

https://huagongshe.com/reaction/1786393

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-4-nitroanisoleHCID 78870—
SolventHydrochloric AcidHCID 313—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product2-Bromo-4-nitrophenolHCID 2210952.3%

Reaction Conditions

Temperature115 °C

Reaction Steps

2-Bromo-4-nitroanisole (20 g, 0.086 mol) was dissolved in DMF (414 mL) at rt under N2. Sodium ethylthiolate (17.4 g, 0.207 mol) was added and the reaction mixture was warmed to 115° C. for 2 h. The reaction was cooled to rt and diluted with EtOAc (200 mL) and 1 M HCl (aq., 200 mL). The phases were separated, and the desired product was extracted into 1 M NaOH (aq, 150 mL×3). The basic aqueous extracts were combined and acidified using conc. HCl. The desired product was extracted from the acidic aqueous solution using EtOAc (250 mL×2). The combined organic layers were washed with brine and dried over sodium sulfate. The volatiles were removed in vacuo to afford a light brown semi-solid (9.8 g, 52% yield). 1H NMR (DMSO-d6) δ 8.33 (m, 1H); 8.09 (m, 1H); 7.07 (d, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07507741B2
Source datasetuspto-grants-2009_03
ORD IDord-98477e2db71c432cafa206b1cb5ed9e6
Source noteuspto-grants-2009_03