HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tert-Butyl nitrite → 2-Methyl-6-nitrothioanisole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tert-Butyl nitrite | HCID 10906 | — |
| Reactant | 2-Methyl-6-nitroaniline | HCID 11298 | — |
| Reactant | Dimethyl Disulfide | HCID 12232 | — |
| Catalyst | Copper | HCID 23978 | — |
| Product | 2-Methyl-6-nitrothioanisole | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07196229B2 |
| Source dataset | uspto-grants-2007_03 |
| ORD ID | ord-58ea4b3780c3416b8f4265eca50208fb |
| Source note | uspto-grants-2007_03 |