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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 266528Erstellt: 26. Oktober 2026

Isopropyl iodide → Methyl 3-amino-2-methyl-6-(1-methylethylsulphenyl)-benzoate

https://huagongshe.com/reaction/266528

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIsopropyl iodideHCID 6362—
EduktSodium SulfideHCID 14804—
EduktMethyl 3-amino-2-methyl-6-thiocyanatobenzoateHCID 14801188—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
ProduktMethyl 3-amino-2-methyl-6-(1-methylethylsulphenyl)-benzoateHCID 5417721975,3%

Reaktionsbedingungen

Temperatur5 °C

Reaktionsschritte

A suspension of methyl 3-amino-2-methyl-6-thiocyanatobenzoate (22.2 g) in ethanol was added to a solution of sodium sulphide (26.6 g) in water. The resultant mixture was stirred at room temperature for 1 hour and then cooled to 5° C. 2-Iodopropane (19.36 g) was added and the mixture was allowed to warm to room temperature and stirred for 2 hours. It was evaporated to dryness and the residue was suspended in aqueous sodium chloride solution and extracted with dichloromethane. The organic layer was dried (MgSO4) and filtered. The filtrate was evaporated to dryness to give methyl 3-amino-2-methyl-6-(1-methylethylsulphenyl)benzoate (18 g) as a yellow oil NMR(CDCl3) 1.2(d,6H) 2.0(s,3H) 3.0(m, 1H) 3.8(bs,2H) 3.9(s, 1H) 6.5(d, 1H) 7.0(d, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05650533
Quelldatensatzuspto-grants-1997_07
ORD IDord-351fc97011b0471bb2bcb5843ff1e216
Quellennotizuspto-grants-1997_07