HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hexane → 1-[2-Fluoro-5-(trifluoromethyl)phenyl]-3-(4-iodophenyl)urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | 4-Iodoaniline | HCID 10893 | — |
| Reactant | 2-Fluoro-5-(trifluoromethyl)phenyl isocyanate | HCID 2733380 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 1-[2-Fluoro-5-(trifluoromethyl)phenyl]-3-(4-iodophenyl)urea | HCID 69008564 | 82% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a solution of 4-iodoaniline (438 mg, 2.0 mmol) in 15.0 mL 1,2-dichloroethane at rt was added 2-fluoro-5-(trifluoromethyl)phenyl isocyanate (0.304 mL, 2.1 mmol). After 50 minutes 3 mL hexane was added, the mixture cooled to 0° C., the precipitant filtered and rinsed with 10% EtOAc/hexane to give the title compound as a light purple solid (692 mg, 82%). 1H NMR (DSMO-d6) δ: 9.26 (s, 1H), 8.90 (d, J=2.9 Hz, 1H), 8.59 (dd, J=7.3, 2.3 Hz, 1H), 7.60-7.65 (m, 2H), 7.46-7.54 (m, 1H), 7.36-7.43 (m, 1H), 7.29-7.34 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09321721B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-2fb3166e76934f01b725727bffcfa311 |
| Source note | uspto-grants-2016_04 |