HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1065077Generated: October 27, 2026
Phenol → 2,6-Bis(1-methylethyl)-4-phenoxybenzenamine
https://huagongshe.com/reaction/1065077
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phenol | HCID 996 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-Bromo-2,6-diisopropylaniline | HCID 11780114 | — |
| Catalyst | Cupric Chloride | HCID 24014 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 2,6-Bis(1-methylethyl)-4-phenoxybenzenamine | HCID 13272139 | — |
Reaction Steps
48.9 g of phenol are dissolved in 500 ml of xylene, and to this solution are added 30.2 g of pulverised potassium hydroxide in an atmosphere of nitrogen. The reaction mixture is stirred and heated to boiling point, while continuously distilling off the water that is formed. After addition of 0.6 g of copper chloride and 100 g of 2,6-diisopropyl-4-bromoaniline, the mixture is stirred for 8 hours at 150°-155° C., then cooled, and filtered with suction. The filtrate is washed with 15% sodium hydroxide solution (150 ml) and with two 150 ml portions of water. The organic phase is separated and dried over sodium sulfate. The solvent is removed by distillation and the product is distilled, affording the compound of the formula ##STR5## with a boiling point of 103°-104° C./0.01 torr and a melting point of 71°-72° C. (after recrystallisation from hexane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04328247 |
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| Source dataset | uspto-grants-1982_05 |
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| ORD ID | ord-4d8daaab3efd42b2bf6627c5cdbd8b4e |
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| Source note | uspto-grants-1982_05 |
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