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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53267Generated: October 25, 2026

p-Toluenesulfonic acid → t-Butylphenol 2-Phenyl-2-oxazoline

https://huagongshe.com/reaction/53267

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant2-Tert-ButylphenolHCID 6923—
Reactant2-Phenyl-2-oxazolineHCID 244030—
SolventTetrahydrofuranHCID 8028—
Productt-Butylphenol 2-Phenyl-2-oxazolineHCID 86750688—

Reaction Conditions

Temperature170 °C

Reaction Steps

A pure sample of the addition product of t-butylphenol and 2-phenyl-2-oxazoline was obtained for comparative purposes as follows: in a side-armed test tube, 2.94 grams 2-phenyl-2-oxazoline and 3.00 grams t-butyl phenol were combined with 0.08 gram pTSA. The stirred mixture was heated under nitrogen at 170° C. for 16 hours. Pure amide ether addition product [B] was obtained from the reaction mixture by column chromatography on silica gel. The crude reaction mixture was taken up in tetrahydrofuran and introduced onto the column, which was subsequently eluted with 1/1 (v/v) hexane/ethyl acetate. Desired fractions were identified by thin layer chromatography, and the product structure was confirmed by 1H and 13C NMR. The reaction is outlined in Scheme 1. ##STR3##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05618896
Source datasetuspto-grants-1997_04
ORD IDord-6b81bcb965514342b8020cef002faef9
Source noteuspto-grants-1997_04