Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethoxysilane | HCID 13830 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Benzyl acetone | HCID 17355 | — |
| Catalyst | Dysprosium tripropan-2-olate | HCID 13033546 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Phenyl-2-butanol | HCID 61302 | 52% |
Reaction Steps
A dry Schlenk tube under argon was charged with 51 mg (0.15 mmol) of dysprosium (III) isopropoxide. Triethoxysilane (1.4 mL, 7.5 mmol) was added, and the reaction mixture was heated to 60° C. After 0.5 hours, 4-phenyl-2-butanone (450 μL, 3 mmol) was added. After 24 hours, the reaction was complete, as determined by GLC analysis of a aliquot taken from the reaction mixture. THF (8 mL) and aqueous NaOH (1 N, 15 mL) were added, and the mixture was stirred vigorously for 12 hours. After work-up as in Example 13, the crude material was purified by flash chromatography (ether:hexane=3:7) to afford 234 mg (52% yield) of 4-phenyl-2-butanol (>95% pure by 1H-NMR analysis).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05220020 |
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| Source dataset | uspto-grants-1993_06 |
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| ORD ID | ord-63e4f63e66e54ed8bdc2bf16ca59989b |
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| Source note | uspto-grants-1993_06 |
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