Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4-Hydroxybenzyl Alcohol | HCID 125 | — |
| Edukt | Pyridine | HCID 1049 | — |
| Edukt | Phosphorus tribromide | HCID 24614 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Bromocresol | HCID 41663 | — |
Reaktionsschritte
To a stirred solution of PBr3 (1.38 g, 5.0 mmol) in dry THF (2 ml) at −5° C. was added a solution of dry pyridine (0.201 ml) in dry THF (0.4 ml). A solution of 4-Hydroxybenzyl alcohol (1.89 g, 15.2 mmol) in dry THF (23 ml) was added drop wise to the reaction mixture. The reaction mixture was allowed to stand at room temperature for 18 hours, then diluted with THF and filtered through celite pad. The filtrate was evaporated, the resulting semisolid was redissolved in dry toluene (16 ml). The solution was maintained at −20° C. for 2 hours, and then filtered through celite pad to provide the title compound as a light yellow solution which was used without further purification.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US06858602B2 |
|---|
| Quelldatensatz | uspto-grants-2005_02 |
|---|
| ORD ID | ord-7b0b35eb3ff04b7a9a9875af0715cb58 |
|---|
| Quellennotiz | uspto-grants-2005_02 |
|---|