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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Benzene, 1,3-dichloro-2-iodo-5-nitro- | HCID 112948 | — |
| Reactant | 4-Fluoro-3-methylphenol | HCID 2737394 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 3,5-Dichloro-4-(4-fluoro-3-methyl-phenoxy)-nitrobenzene | HCID 18614274 | 82.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06326398B1 |
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| Source dataset | uspto-grants-2001_12 |
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| ORD ID | ord-89b4dd4e09db41f89bce9bc684e80f25 |
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| Source note | uspto-grants-2001_12 |
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