Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | HCID 21412879 | HCID 21412879 | — |
| Catalyst | Sulfuric Acid | HCID 1118 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21412894 | HCID 21412894 | 671.4% |
Reaction Steps
263 g of 2-chloro-3-methyl-4-hydroxy-6-[α-(2,4-di-tert-amylphenoxy)butyramido]phenol and 5 g of sodium acetate were dissolved in 500 ml of glacial acetic acid and heated for 30 minutes at 80° C. After cooling the reaction solution, 1.5 l of water and 2 - 3 drops of concentrated sulfuric acid were added thereto and the system stirred at room temperature for 30 minutes and the diacetyl compound was deposited in the form of an oil. The oil was dissolved in 2 l of dimethylformamide and a solution of 1 l of water, 250 g of sodium carbonate and 1 l of methanol was added thereto and the system stirred at room temperature for 1 hour. 150 ml of concentrated hydrochloric acid was then added to the mixture and the mixture was poured into water and the precipitated crystals were recrystallized from methanol to obtain 212 g of the desired compound having a melting point of 188° to 190° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04046573 |
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| Source dataset | uspto-grants-1977_09 |
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| ORD ID | ord-295a254430f0417e8dbb109fc369cd03 |
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| Source note | uspto-grants-1977_09 |
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