Réaction #77959

Équation de réaction

tert-butyl nitrite

dimethyl disulfide

2-methyl-6-nitroaniline

dimethyl disulfide

→

2-methyl-6-nitrothioanisole

Conditions de réaction

Traitement

1. 1
   FiltrationFor work-up, the solid is filtered off with suction
2. 2
   workup.ADDITIONthe filtrate is diluted with methylene chloride
3. 3
   Extractionextracted with dilute hydrochloric acid
4. 4
   LavageThe organic phase is washed with saturated aqueous NaHCO3 solution
5. 5
   Séchagedried over sodium sulfate
6. 6
   Filtrationfiltered off
7. 7
   Concentrationconcentrated
8. 8
   AutreExcess dimethyl disulfide is removed under oil pump vacuum

Mode opératoire

226 g (1.97 mol) of tert-butyl nitrite and 100 g of copper powder are initially charged in 300 ml of dimethyl disulfide, and a solution of 200 g (1.32 mol) of 2-methyl-6-nitroaniline in 700 ml of dimethyl disulfide is added dropwise at from 50 to 55° C. The mixture is subsequently stirred at 75° C. for 8 hours. For work-up, the solid is filtered off with suction and the filtrate is diluted with methylene chloride and extracted with dilute hydrochloric acid. The organic phase is washed with saturated aqueous NaHCO3 solution, dried over sodium sulfate, filtered off and concentrated. Excess dimethyl disulfide is removed under oil pump vacuum. This gives 271 g (99%) of a dark-red oil, purity according to HPLC 87%.

Source