HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
3-Hydroxybenzaldehyde → 3-[(2,4,6-Trimethyl-benzylamino)-methyl]-phenol
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 3-Hydroxybenzaldehyde | HCID 101 | — |
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | 2,4,6-Trimethylbenzylamine | HCID 458433 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | 3-[(2,4,6-Trimethyl-benzylamino)-methyl]-phenol | HCID 68982186 | — |
Reaktionsschritte
3-Hydroxy-benzaldehyde (1.22 g, 0.01 mol) and 2,4,6-trimethyl-benzylamine (1.19 g, 0.01 mol) were added to methanol (10 mL) and the resulting mixture was stirred overnight. Sodium borohydride (0.45 g, 0.012 mol) was then added, and stirring was continued one hour. The resulting mixture was acidified with 2N HCl and then neutralized with saturated aqueous NaHCO3 solution to yield a gummy solution. The gummy solution was extracted with EtOAc (3×100 mL). The organic layer was washed with brine, dried over sodium sulfate, and concentrated in vacuo to yield a white solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08076358B2 |
| Quelldatensatz | uspto-grants-2011_12 |
| ORD ID | ord-be333cfe5a40457c91984a3e50d1a8c0 |
| Quellennotiz | uspto-grants-2011_12 |