HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Amino-4-tert-butylphenol → 5-(tert-Butyl)-2-methylbenzoxazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Amino-4-tert-butylphenol | HCID 70982 | — |
| Reactant | Ethanimidic acid, methyl ester, hydrochloride (1:1) | HCID 10313100 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-(tert-Butyl)-2-methylbenzoxazole | HCID 12595413 | 24% |
Reaction Steps
In a 100 ml round bottom flask was placed 7.25 g (0.044 mol) of 2-Amino-4-tert-butylphenol, (Aldrich Cat #193282) with 6.0 g (0.055 mol) of Methyl acetimidate hydrochloride (Aldrich Cat #254940) with 50 ml of MeOH. This was refluxed for 4 hours. Then the MeOH was removed under vacuum. This was separated between 50 ml of ether and 50 ml of water. The ether was separated, dried, and removed under vacuum. Then 50 ml of hexanes was added to the resulting solid. Remaining 2-Amino-4-tert-butylphenol was insoluble in hexanes and was removed by filtration. The remaining oil was chromatographed using 2% MeOH/CH2Cl2 to provide 5-tert-butyl-2-methylbenzoxazole (Yield=2 g, 24%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08894976B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-4f8e68d288d241cc9dd11a788066fc17 |
| Source note | uspto-grants-2014_11 |