HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → Phenol, 4-(diphenylamino)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | 4-Methoxytriphenylamine | HCID 9882037 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Phenol, 4-(diphenylamino)- | HCID 11492641 | 81% |
Reaction Steps
To a solution of 4-methoxy-N,N-diphenylaniline (6.0 g, 21.8 mmol) in DCM (40 mL) was slowly added BBr3 (23 mL, 23 mmol) at about −78° C. The mixture was then stirred overnight under argon while it slowly warmed up to room temperature. To the resulting mixture, methanol (70 mL) was added slowly, then stirred for about 3 hours. The mixture was then poured into water and extracted with DCM (2×200 mL). The organic phases were then combined and washed with brine, dried over Na2SO4, loaded on silica gel, and purified by short plug using hexane/ethyl acetate (9:1 to 8:1). The desired fraction was concentrated and washed with hexanes to give a white solid (Compound 7) (4.59 g, in 81% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09343684B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-a237686e1aa24a96b17c9d69cb0d8bb6 |
| Source note | uspto-grants-2016_05 |