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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397156Generated: October 26, 2026

Tert-Butyl nitrite → 2-Methyl-6-nitrothioanisole

https://huagongshe.com/reaction/397156

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-Butyl nitriteHCID 10906—
Reactant2-Methyl-6-nitroanilineHCID 11298—
ReactantDimethyl DisulfideHCID 12232—
CatalystCopperHCID 23978—
Product2-Methyl-6-nitrothioanisoleHCID 18757272—

Reaction Conditions

Temperature75 °C

Reaction Steps

226 g (1.97 mmol) 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 50-55° C. The mixture is then stirred at 75° C. for 8 hours. For work-up, the solid is filtered off with suction and the solution 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 using a rotary evaporator. Excess dimethyl disulfide is removed under oil pump vacuum. This gives 271 g (99%) of a dark-red oil, purity according to HPLC 87%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06608209B2
Source datasetuspto-grants-2003_08
ORD IDord-40b4362529454619938db5cb473be91e
Source noteuspto-grants-2003_08