Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 19068449 | HCID 19068449 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 10735330 | HCID 10735330 | 47% |
Reaction Steps
To 6.00 g (16.3-mmol) of N,N'-bis(2-hydroxy-1,1-dimethylethyl)-2,3-dimethoxy-1,4-phenylenedicarboxamide, was added 7.0 mL (96.0 mmol) of thionyl chloride. The mixture was stirred at room temperature for 3 hours. Further thereto, 7.0 mL (96.0 mmol) of thionyl chloride was added, and the mixture was stirred at room temperature for one hour. The reaction solution was poured into 50 mL of ether. The supernatant liquid was removed by decantation. Aqueous 10% sodium hydroxide solution was added to the residue to bring the pH to 8. It was extracted with ether, and was dried over anhydrous sodium sulfate. The solvent was removed by distillation, and the residue was purified by silca gel column chromatography (methylene chloride:ethanol=20:1) to obtain 2.52 g (47%) of 2,2'-(2,3-dimethoxy-1,4-phenylene)-bis (4,4-dimethyl-2-oxazoline) in a colorless crystal state.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05786486 |
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| Source dataset | uspto-grants-1998_07 |
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| ORD ID | ord-16d0cfef401645d7af9378c73ce3ad00 |
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| Source note | uspto-grants-1998_07 |
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