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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49681Generated: October 27, 2026

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

https://huagongshe.com/reaction/49681

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 numberUS06706886B2
Source datasetuspto-grants-2004_03
ORD IDord-386dca9a8cd840e7b83c2ebe367202a1
Source noteuspto-grants-2004_03