Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 10735330 | HCID 10735330 | — |
| Reactant | HCID 178418443 | HCID 178418443 | — |
| Product | HCID 10496538 | HCID 10496538 | 100% |
Reaction Steps
In 20 mL of anhydrous tetrahydrofuran, was dissolved 2.00 g (6.02 mmol) of 2,2'-(2,3-dimethoxy-1,4-phenylene)-bis(4,4-dimethyl-2-oxazoline). Thereto, 16.4 mL of 0.92M ethylmagnesium bromide solution (15.1 mmol) in tetrahydrofuran was added dropwise with ice cooling in 30 minutes, and the mixture was stirred at room temperature for 2 hours. To the reaction liquid, were added successively 10 mL of aqueous saturated ammonium chloride solution and 30 mL of water. The product was extracted from the mixture with ether, washed with a saturated sodium chloride solution, and dried over anhydrous sodium sulfate. The solvent was removed by distillation. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=2:1) to obtain 1.98 g (100%) of 2,2'-(2,3-diethyl-1,4-phenylene)-bis(4,4-dimethyl-2-oxazoline) in a colorless prism 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-cf199668c659453a89f35eb3fe9ed741 |
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| Source note | uspto-grants-1998_07 |
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