HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1028636Generated: October 30, 2026
Iodine → 2-iodine-4 -(trifluoromethyl) anisole
https://huagongshe.com/reaction/1028636
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Tert-Butyl nitrite | HCID 10906 | — |
| Reactant | 2-Methoxy-5-(trifluoromethyl)aniline | HCID 600637 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-iodine-4 -(trifluoromethyl) anisole | HCID 18706296 | — |
Reaction Steps
To a stirred solution of 2-methoxy-5-(trifluoromethyl)aniline (500 mg, 2.62 mmol) in CH2Cl2 (10 mL) was added t-butyl nitrite (467 μL, 3.93 mmol). The reaction was stirred for 5 min prior to addition of iodine (1.3 g, 5.24 mmol), and then heated at 70° C. for 2 h. The reaction was cooled, diluted with CH2Cl2 (10 mL), washed with sat. Na2S2O3 (10 mL) and brine (10 mL), dried over Na2SO4, filtered and concentrated in vacuo. The crude product was purified by flash silica gel chromatography (hexanes) to afford 2-iodo-1-methoxy-4-(trifluoromethyl)benzene as a light yellow solid. 1H NMR (CDCl3, 500 MHz): δ 8.05 (d, J=2 Hz, 1 H), 7.61 (dd, J=8.7, 1.8 Hz, 1 H), 6.89 (d, J=8.7 Hz, 1 H), 3.97 (s, 3 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08735435B2 |
|---|
| Source dataset | uspto-grants-2014_05 |
|---|
| ORD ID | ord-c46a75d80afd45b0b757b068b936273c |
|---|
| Source note | uspto-grants-2014_05 |
|---|