Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Trichloroacetonitrile | HCID 11011 | — |
| Reactant | 3-Buten-2-ol | HCID 11716 | — |
| Reactant | Potassium hydride | HCID 82127 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 54454059 | HCID 54454059 | — |
Reaction Steps
A solution of 3-butene-2-ol (8.7 mL, 100 mmol) in THF (50 mL) was added to potassium hydride (KH, 600 mg, 15 mmol) over 15 min. The resulting alkoxide solution was added to a stirred solution of trichloroacetonitrile (10.03 mL, 100 mmol) in ether (100 mL) at −10° C. The solution was stirred at 0° C. for 3 h, followed by removal of solvent under reduced pressure (temperature <25° C.); pentane (400 mL) and methanol (1 mL) were added, and the mixture filtered. Concentration afforded a yellow oil (17.4 g). The oil was dissolved in xylene (450 mL) and refluxed for 2.5 h. The solvent was removed to yield 16.8 g of the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06448286B1 |
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| Source dataset | uspto-grants-2002_09 |
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| ORD ID | ord-cfe7470750084ce7bc83a200a0f73ad1 |
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| Source note | uspto-grants-2002_09 |
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