Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Dimethoxymethane | HCID 8020 | — |
| Reactant | Phenol, 6-(1,1-dimethylethyl)-2,3-dimethyl- | HCID 170766 | — |
| Product | HCID 20361461 | HCID 20361461 | — |
Reaction Steps
30 Grams of 6-tert.-butyl-2,3-dimethylphenol dissolved in 100 ml of toluene was added to 2.7 ml of concentrated hydrochloric acid containing 3.3 ml of concentrated sulfuric acid at 5° to 10° C. 26 grams of methylal was added dropwise to the above vigorously stirred dispersion over a period of about 15 minutes after which the reaction mixture was heated at 36° to 37° for 2 hours while bubbling anhydrous gaseous chloride through the reaction mixture. The reaction temperature was allowed to drop to 27° during the following 2 hours while continuing to bubble anhydrous hydrogen chloride thorugh the reaction mixture. The acidic aqueous phase was separated from the reaction mixture after being extracted with toluene and the combined toluene phases washed well with cold water and dried over anhydrous sodium sulfate. After filtering free of drying agent, the clear filtrate was freed of solvent by distillation at reduced pressures the resulting residue being crystallized from petroleum ether yielding the desired compound in the form of light yellow crystals melting at 92° to 95° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04081475 |
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| Source dataset | uspto-grants-1978_03 |
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| ORD ID | ord-c32cf8cc5cb445c3aa1b299ac6a1faee |
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| Source note | uspto-grants-1978_03 |
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