HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393392Generated: October 29, 2026
Water → 4-(2,6-Dibromo-4-nitrophenoxy)-2-isopropylanisole
https://huagongshe.com/reaction/393392
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1,3-Dibromo-2-iodo-5-nitrobenzene | HCID 10158279 | — |
| Reactant | 3-Isopropyl-4-methoxyphenol | HCID 11332675 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(2,6-Dibromo-4-nitrophenoxy)-2-isopropylanisole | HCID 11744209 | — |
Reaction Steps
3-Isopropyl-4-methoxyphenol (197.2 g, 1.19 moles) was dissolved in dimethylformamide (4 L). The mixture was stirred while the reaction vessel was cooled in an icewater bath. Sodium hydroxide (1.278 L of 1.0M aqueous solution, 1.278 moles) was added while maintaining the temperature of the reaction mixture below 35° C. 1,3-Dibromo-2-iodo-5-nitrobenzene (400.0 g, 0.983 moles) dissolved in dimethylformamide (portion of 4 L) was added to the reaction mixture over approximately 45 min. The reaction mixture was stirred at 20° to 25° C. for 24 h. Deionized water (2 L) was added over 2 h and the reaction mixture was cooled to 5° C. The resulting crystals of 4-(2,6-dibromo-4-nitrophenoxy)-2-isopropylanisole (405.4 g, 92.6%) were recovered by filtration and dried for 48 h by evaporation under air flow at room temperature.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06806381B2 |
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| Source dataset | uspto-grants-2004_10 |
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| ORD ID | ord-fd5e89f055fa435d8087537ffa6ecfb9 |
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| Source note | uspto-grants-2004_10 |
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