Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 915299Generated: October 31, 2026

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

https://huagongshe.com/reaction/915299

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, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07265123B2
Source datasetuspto-grants-2007_09
ORD IDord-2b80ba0698744c94809a46f89a433b9a
Source noteuspto-grants-2007_09