HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2951Erstellt: 23. Oktober 2026
2-Tert-Butylphenol → 3-(tert-Butyl)-4-hydroxybenzaldehyde
https://huagongshe.com/de/reaction/2951
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 2-Tert-Butylphenol | HCID 6923 | — |
| Edukt | Phosphorus oxychloride | HCID 24813 | — |
| Edukt | N-Methylformanilide | HCID 66737 | — |
| Produkt | 3-(tert-Butyl)-4-hydroxybenzaldehyde | HCID 3017618 | 22,6% |
Reaktionsschritte
Into 101.5 g of N-methylformanilide was added dropwise with cooling 107 g of phosphoryl chloride over a period of 15 minutes. The mixture was allowed to warm to room temperature and stirred for 70 minutes. 67.5 g of ortho-t-butylphenol was added and stirred for about 45 minutes after which the mixture was heated to about 50°-60° C. and allowed to stir for 4.5 hours. The reaction mixture was poured into a volume of crushed ice and extracted with chloroform. The aqueous layer was separated and washed again with chloroform. The chloroform layers were combined and extracted with 2000 ml of a 5% potassium hydroxide solution. The aqueous potassium hydroxide layer was separated and added to 1000 ml of chloroform. The pH of the resulting two-phase mixture was adjusted to 3 with concentrated hydrochloric acid with stirring. The resultant layers were separated and the aqueous layer was again extracted with chloroform and dried over sodium sulfate overnight to give 18.1 g of the desired subtitled intermediate.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US05731336 |
|---|
| Quelldatensatz | uspto-grants-1998_03 |
|---|
| ORD ID | ord-2b92740c81364c30af7dcfcac8c1abbd |
|---|
| Quellennotiz | uspto-grants-1998_03 |
|---|