HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1703463Generated: October 30, 2026
Dimethyl Sulfide → 2-[(Methylsulfanyl)methyl]-4-nitroaniline
https://huagongshe.com/reaction/1703463
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfide | HCID 1068 | — |
| Reactant | 4-Nitroaniline | HCID 7475 | — |
| Reactant | Tert-Butyl hypochlorite | HCID 521297 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-[(Methylsulfanyl)methyl]-4-nitroaniline | HCID 326707 | — |
Reaction Steps
The starting material is prepared as follows: The solution of 23.4 g of t-butylhypochlorite in 20 ml of methylene chloride is added to that of 30.0 g of 4-nitroaniline and 27.0 g of dimethyl thioether in 650 ml of acetonitrile and 200 ml of methylene chloride while stirring at -40° under nitrogen. After 4 hours the temperature is raised to -20° and maintained there for three hours. After the addition of 30 g of sodium methoxide in 100 ml of methanol the mixture is refluxed for 15 hours, cooled, filtered and evaporated. The residue is dissolved in diethyl ether and filtered through a silica gel column to remove any unreacted 4-nitroaniline as its benzenesulfonate following addition of 17.4 g of benzenesulfonic acid. The filtrate is evaporated and the residue recrystallized from ethanol, to yield the 4 -nitro-2-methylmercaptomethylaniline melting at 72°-77°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04124593 |
|---|
| Source dataset | uspto-grants-1978_11 |
|---|
| ORD ID | ord-a51de74925984c479b3d908876a7eb77 |
|---|
| Source note | uspto-grants-1978_11 |
|---|