HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 3,5-Di-tert-butyl-4-hydroxybenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Hexamethylenetetramine | HCID 4101 | — |
| Reactant | 2,6-Di-tert-butylphenol | HCID 31405 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 3,5-Di-tert-butyl-4-hydroxybenzaldehyde | HCID 73219 | — |
Reaction Steps
2,6-di-tert-butylphenol was dissolved in glacial acetic acid. Subsequently, urotropin and water were added, and the reaction mixture heated at not more than 2° C. below the reflux temperature for 4 to 5 hours. The precipitated product was filtered off and washed with water and methanol, and dried on a rotary evaporator. The molar ratios of the reactants used and also the determined yields of 3,5-di-tert-butyl-4-hydroxybenzaldehyde, based on 2,6-di-tert-butylphenol, are shown in Table 4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08212081B2 |
| Source dataset | uspto-grants-2012_07 |
| ORD ID | ord-95ebbb52671e4d0dbde64ecec9231898 |
| Source note | uspto-grants-2012_07 |