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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2268126Generated: November 1, 2026

Ethyl Acetate → 3,5-Dichloro-4-(4-fluoro-3-methyl-phenoxy)-nitrobenzene

https://huagongshe.com/reaction/2268126

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium HydroxideHCID 14797—
ReactantBenzene, 1,3-dichloro-2-iodo-5-nitro-HCID 112948—
Reactant4-Fluoro-3-methylphenolHCID 2737394—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product3,5-Dichloro-4-(4-fluoro-3-methyl-phenoxy)-nitrobenzeneHCID 1861427482.9%

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of 3-methyl-4-fluorophenol (99 mg, 0.79 mmol), potassium hydroxide (53 mg, 0.94 mmol), 4-iodo-3,5-dichloro-nitrobenzene (250 mg, 0.79 mmol) and 4A° molecular sieves (75 mg) in N-methylpyrolidinone (3 mL) was stirred at 130° C. for 2 h. The reaction mixture was poured into ice cold 1 N HCI (20 mL) and EtOAc (25 mL) was added. The EtOAc phase was separated and washed with 1 N HCI (3×25 mL) and brine (25 mL). The EtOAc solution was dried over Na2SO4, filtered and concentrated. The residue was purified by preparative TLC (Hexanes: CH2CI2=7:3) to afford 3,5-dichloro-4-(4-fluoro-3-methyl-phenoxy)-nitrobenzene (207 mg). MS Calc.: 315.0 Found: 315.0 (M).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06326398B1
Source datasetuspto-grants-2001_12
ORD IDord-89b4dd4e09db41f89bce9bc684e80f25
Source noteuspto-grants-2001_12