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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339298Generated: October 26, 2026

2-Amino-4-tert-butylphenol → 5-(tert-Butyl)-2-methylbenzoxazole

https://huagongshe.com/reaction/339298

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-4-tert-butylphenolHCID 70982—
ReactantEthanimidic acid, methyl ester, hydrochloride (1:1)HCID 10313100—
SolventMethanolHCID 887—
Product5-(tert-Butyl)-2-methylbenzoxazoleHCID 1259541324%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08894976B2
Source datasetuspto-grants-2014_11
ORD IDord-4f8e68d288d241cc9dd11a788066fc17
Source noteuspto-grants-2014_11