HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 326990Generated: October 30, 2026
Dimethyl Sulfide → 2-Amino-3-(methylthiomethyl)benzotrifluoride
https://huagongshe.com/reaction/326990
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfide | HCID 1068 | — |
| Reactant | 2-(Trifluoromethyl)aniline | HCID 6922 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Amino-3-(methylthiomethyl)benzotrifluoride | HCID 2735934 | — |
Reaction Steps
Dimethylsulfide, 16 ml, was syringed all at once into a solution of 25.0 grams (g) of 2-(trifluoromethyl)aniline in 400 milliliters (ml) of methylene chloride. The reaction solution was cooled to 15° C. and 29.0 g of N-chlorosuccinimide was added in small portions over a 20 minute period at such a rate that the reaction temperature did not exceed 20° C. The reaction mixture was stirred at 15° C. for 15 minutes, then 30.4 ml of triethylamine was added dropwise over 15 minutes at such a rate that the temperature did not exceed 15° C. After an additional five minutes of stirring, the reaction was refluxed overnight, allowed to cool to room temperature, washed with two 200 ml portions of 10% sodium hydroxide, the organic phase separated, dried with magnesium sulfate and filtered. The remainder of the solvent was distilled off to yield 35.8 g of the crude desired product which was used without any additional purification in subsequent reactions.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05272128 |
|---|
| Source dataset | uspto-grants-1993_12 |
|---|
| ORD ID | ord-9bd097b9552242febf8008a8323bf7ca |
|---|
| Source note | uspto-grants-1993_12 |
|---|