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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434225Generated: October 26, 2026

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

https://huagongshe.com/reaction/434225

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 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%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06670482B2
Source datasetuspto-grants-2003_12
ORD IDord-805a7843e6ed4aa98af451ea83f9a19c
Source noteuspto-grants-2003_12