HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,6-Di-tert-butylphenol → Tetrabutylammonium 2,6-di-t-butylphenoxide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,6-Di-tert-butylphenol | HCID 31405 | — |
| Reactant | Tetrabutylammonium Hydroxide | HCID 2723671 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Tetrabutylammonium 2,6-di-t-butylphenoxide | HCID 9911496 | — |
Reaction Steps
A solution of 22.69 g (110 mmol, 1.1 equivalents) of 2,6-di-t-butylphenol in 10 mL of toluene was treated with 100 mL (100 mmol) of a 1M solution of tetrabutylammonium hydroxide in methanol under nitrogen with stirring at ambient temperature. The resulting dark green solution was stirred for 1 hour and concentrated under vacuum to a thick residue. Two 100 mL portions of toluene were added and removed by evaporation under vacuum yielding 52.08 g of wet, crude title compound as a green solid which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06198000B1 |
| Source dataset | uspto-grants-2001_03 |
| ORD ID | ord-1f616a1b34804a20a516a3c5cee642f1 |
| Source note | uspto-grants-2001_03 |