HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 3,5-DI-Tert-butyl-4-hydroxybenzylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | N-(3,5-di-tert-butyl-4-hydroxybenzyl)formamide | HCID 13438362 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3,5-DI-Tert-butyl-4-hydroxybenzylamine | HCID 601078 | 97% |
Reaction Steps
9.81 g (37.3 mmol) N-formyl-3,5-di-tert.butyl-4-hydroxybenzyl-amine was dissolved in 24 mL dioxane and 7.2 mL concentrated hydrochloric acid. The mixture was heated to reflux for one hour. The mixture was allowed to cool down to room temperature and diluted with 50 mL water. The mixture was made alkaline, using a 10% ammonia solution. 3,5-di-tert.butyl-4-hydroxybenzyl amine precipitated from the medium, was isolated by filtration and dried. 8.5 g (97%) of 3,5-di-tert.butyl-4-hydroxybenzyl amine was isolated (m.p.: 159-9° C.). 3,5-di-tert.butyl-4-hydroxybenzyl amine has a tendency to lose ammonia upon heating, forming the corresponding di- and tribenzyl derivatives.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09416287B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-66bcd1c5771f43a79f8fdb46f649fdc4 |
| Source note | uspto-grants-2016_08 |