Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Bromo-2,5-dichlorophenol | HCID 16022 | — |
| Reactant | HCID 13102542 | HCID 13102542 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 12881150 | HCID 12881150 | — |
Reaction Steps
A mixture of 28.4 gm of 4,5-dichloro-2-nitro-1-phenoxy-benzene, 24.2 gm of 2,5-dichloro-4-bromo-phenol, 10 ml of 10 N sodium hydroxide and 80 ml of dimethylsulfoxide was stirred for 5 hours at 100° C. Thereafter, the reaction mixture was stirred into 700 ml of 1 N sodium hydroxide, the mixture was allowed to stand overnight at room temperature, the liquid phase was decanted, and the precipitated product was taken up in chloroform. The chloroform solution was washed with water, dried with sodium sulfate and evaporated, and the residue was recrystallized from a mixture of 200 ml ethanol and 2 ml dimethylformamide. 36.5 gm (75% of theory) of the light yellow crystalline title compound, m.p. 85° C., were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04364875 |
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| Source dataset | uspto-grants-1982_12 |
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| ORD ID | ord-55237b03e38b4bd9a6c4a47b4978979c |
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| Source note | uspto-grants-1982_12 |
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