HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 70075Erstellt: 24. Oktober 2026
((4-Hydroxy-3-methylphenyl)sulfanyl)formonitrile → 4-Mercapto-2-methylphenol
https://huagongshe.com/de/reaction/70075
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | ((4-Hydroxy-3-methylphenyl)sulfanyl)formonitrile | HCID 220928 | — |
| Edukt | Aluminium lithium hydride | HCID 21226445 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 4-Mercapto-2-methylphenol | HCID 11320974 | — |
Reaktionsschritte
In a 500 ml three-necked flask, to a stirred mixture of lithium aluminum tetrahydride (LiAlH4, 3.5 g, 92.2 mmol) and tetrahydrofuran (THF, 50 ml) was added dropwise a solution of 3-methyl-4-hydroxy-phenyl thiocyanic acid (6.13 g, 37.1 mmol) in tetrahydrofuran (THF, 30 ml) at 0° C. After 30 min of stirring at 0° C., the mixture was warmed up to room temperature and then stirred for 1 hour at room temperature. The reaction was quenched by adding ethanol (10 ml), The value of pH of the mixture was adjusted to 3-4 by adding 6 M hydrochloric acid in an ice water bath. Then the aqueous layer was extracted with ethyl acetate (3×100 ml). The combined organic layer was dried over anhydrous magnesium sulfate, filtrated, and evaporated in vacuo to give a crude product 4-hydroxy-3-methyl thiophenol as yellow oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US08822519B2 |
|---|
| Quelldatensatz | uspto-grants-2014_09 |
|---|
| ORD ID | ord-9237ec10850e41e4ad0dbfd9462ebd5c |
|---|
| Quellennotiz | uspto-grants-2014_09 |
|---|