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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 460501Generated: October 26, 2026

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

https://huagongshe.com/reaction/460501

Reaction equation

Participants

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

Reaction Steps

160 g of copper powder and 500 ml of dimethyl disulfide were added to 357 g (3.12 mol) of tert-butyl nitrite. At 50–52° C., a solution of 316 g (2.08 mol) of 2-methyl-6-nitroaniline in 1600 ml of dimethyl disulfide was added dropwise, and the mixture was stirred at 50–55° C. for 4 hours. After cooling, the reaction mixture was filtered off with suction through kieselguhr, and dichloromethane was added to the filtrate. The organic phase was washed with dilute hydrochloric acid and then with water and subsequently dried over magnesium sulfate. Concentration under high vacuum gave 452 g of 2-methyl-6-nitrothioanisole as a red-black oil which was used for the next reaction step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07196229B2
Source datasetuspto-grants-2007_03
ORD IDord-58ea4b3780c3416b8f4265eca50208fb
Source noteuspto-grants-2007_03