Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 3,4-Dimethylphenol | HCID 7249 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4,4'-Dimethoxybenzoin | HCID 95415 | — |
| Product | HCID 20375429 | HCID 20375429 | — |
Reaction Steps
160 g of 73% strength aqueous sulphuric acid are added dropwise to a mixture of 54.5 g of 1,2-di-(4-methoxyphenyl)-2-oxo-ethanol (p-anisoin) and 73 g of 3,4-dimethylphenol and the mixture is heated at 130°-135° for 20 minutes and then cooled to 20°. The reaction mixture is rendered alkaline by adding an aqueous solution of sodium hydroxide and is heated under reflux and then cooled. It is extracted twice with ethyl acetate; the combined organic extracts are washed with a 2 N aqueous solution of sodium hydroxide and with water, dried over sodium sulphate and filtered and the filtrate is concentrated to half its volume and cooled. The crystalline precipitate is filtered off and recrystallised from ethyl acetate and gives 2,3-di-(4-methoxyphenyl)-5,6-dimethylbenzofurane, melting point 153°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04187234 |
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| Source dataset | uspto-grants-1980_02 |
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| ORD ID | ord-c45cd28e8b06426ea1409d93887947de |
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| Source note | uspto-grants-1980_02 |
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