HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Amino-4-methylphenol → N-(4-Bromophenyl)-5-methyl-1,3-benzoxazol-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Amino-4-methylphenol | HCID 7264 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Bromophenyl isothiocyanate | HCID 16133 | — |
| Catalyst | Copper Sulfate | HCID 24462 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(4-Bromophenyl)-5-methyl-1,3-benzoxazol-2-amine | HCID 21985825 | 81.2% |
Reaction Steps
2-Amino-4-methylphenol (1.15 g, 9.34 mmol) was added to a solution of 4-bromophenyl isothiocyanate (2.00 g, 9.34 mmol) in tetrahydrofuran (35 mL) and the reaction was stirred at room temperature for 16 h. Anhydrous copper (II) sulfate (14.06 g, 88.10 mmol), silica gel (14.06 g), and triethylamine (1.3 mL, 9.34 mmol) were added, and the mixture was stirred at room temperature for 24 h. The reaction was concentrated under reduced pressure and then added to a silica pad and purified using 1:5 ethyl acetate:heptane (2 L) followed by diethyl ether as the eluent to afford N2-(4-bromophenyl)-5-methyl-1,3-benzoxazol-2-amine as a light brown solid (2.30 g, 81%);
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06921763B2 |
| Source dataset | uspto-grants-2005_07 |
| ORD ID | ord-01aea736a1b54e418366820b21c6b3aa |
| Source note | uspto-grants-2005_07 |