HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 1,3-Bis(3,5-di-t-butyl-4-hydroxyphenyl)-2-nitropropane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Nitromethane | HCID 6375 | — |
| Reactant | 2,6-Di-tert-butyl-4-(methoxymethyl)phenol | HCID 6911 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1,3-Bis(3,5-di-t-butyl-4-hydroxyphenyl)-2-nitropropane | HCID 21434884 | — |
Reaction Steps
To a solution of 14.5 g (0.22 mole) of 85% potassium hydroxide in 300 ml of methanol was added in a stream of nitrogen to exclude air 13.4 g (0.22 mole) of nitromethane and 50.0 g (0.2 mole) of 2.6-di-t-butyl-4-methoxymethylphenol. The magenta solution was stirred for one hour at reflux, with exclusion of air. After cooling somewhat, the solution was neutralized with 13 ml of acetic acid and chilled. A thick paste formed which was filtered, washed and dried. The resulting tan powder (48.1 g, mp 152°-154° C) was recrystallized from 500 ml of heptane, after filtering insoluble matter (10.4 g). The yield of tan crystals was 32.3 g, mp 161°-165° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04007159 |
| Source dataset | uspto-grants-1977_02 |
| ORD ID | ord-642b0798f16e43b1a87aed7bc9b05936 |
| Source note | uspto-grants-1977_02 |