HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507038Generated: November 4, 2026
Iodine chloride → 2-Iodo-4-methyl-5-(trifluoromethyl)aniline
https://huagongshe.com/reaction/507038
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine chloride | HCID 24640 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-Methyl-3-(trifluoromethyl)aniline | HCID 2737715 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Sodium Pyrosulfite | HCID 656671 | — |
| Product | 2-Iodo-4-methyl-5-(trifluoromethyl)aniline | HCID 53421146 | 103.1% |
Reaction Steps
Add a solution of iodine monochloride (27.8 g, 171 mmol) in dichloromethane (180 mL) to a solution of 4-methyl-3-trifluoromethylaniline (25.0 g, 143 mmol) and sodium bicarbonate (14.4 g, 171 mmol) in methanol (180 mL) and dichloromethane (730 mL) at room temperature under nitrogen. Stir the mixture for 3 h and dilute the cooled mixture with aqueous sodium metabisulfite (500 mL). Collect the organic phase, and extract the aqueous phase with methylene chloride (200 mL). Wash the combined organic extracts with brine (250 mL), dry over anhydrous sodium sulfate and filter. Remove the solvent under reduced pressure to provide a brown oil, which crystallizes upon standing to afford the title compound as brown needles (44.4 g, >99%), which is used in the next step without purification. APCI MS m/z 302 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07786108B2 |
|---|
| Source dataset | uspto-grants-2010_08 |
|---|
| ORD ID | ord-6ef97865e4da4265acbc33d23ec58cbc |
|---|
| Source note | uspto-grants-2010_08 |
|---|