HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446855Generated: October 30, 2026
2,4-Dichlorophenol → 2,4-Dichloro-1-(2-nitrophenoxy)benzene
https://huagongshe.com/reaction/446855
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,4-Dichlorophenol | HCID 8449 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Fluoro-2-nitrobenzene | HCID 73895 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2,4-Dichloro-1-(2-nitrophenoxy)benzene | HCID 775975 | 91% |
Reaction Steps
A mixture of 1-fluoro-2-nitrobenzene (4.8 mL, 45.42 mmol), potassium carbonate (13.8 g, 0.1 mol) and 2,4-dichloro-phenol (8.16 g, 50.06 mmol) in dry dimethylformamide (70 mL) was stirred at 100° C. for 2 h. Solids were filtered off, and the filtrate was concentrated in vacuo. The residue was partitioned between diethyl ether and 1N sodium hydroxide, the organic layer was washed with 1N sodium hydroxide, water and brine, dried over sodium sulfate, filtered and concentrated in vacuo to yield 11.69 g (91%) of the title compound as a yellowish oil, which solidifies on standing. Mp: 58-59° C. MS (EI) 285.2 (MH+). Lit. [Chem. Heterocycl. Compd. (Engl. Transl.) 11 (1975) 1356-1358] Mp: 57-58° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08481527B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-ae6c409f0ee04ca4b2af36975afc1470 |
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| Source note | uspto-grants-2013_07 |
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