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
Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 2-Tert-Butylphenol | HCID 6923 | — |
| Reactant | 2-Phenyl-2-oxazoline | HCID 244030 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | t-Butylphenol 2-Phenyl-2-oxazoline | HCID 86750688 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05618896 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-6b81bcb965514342b8020cef002faef9 |
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| Source note | uspto-grants-1997_04 |
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