Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 23726637 | HCID 23726637 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23726640 | HCID 23726640 | 98.3% |
Reaction Steps
2.67 g of 163 (5.73 mmol) was dissolved in 35 ml of anhydrous THF, cooled to 0° C. and added with 8.60 ml of TBAF solution (8.60 mmol, 1.5 eq., 1 M/THF). After reacting at RT overnight, 0.5 ml of water was added, followed by stirring for 30 min. Thereafter, the batch was filtered together with a small amount of MTBE over a small amount of silica gel and concentrated. Column chromatography over silica gel (EE/CH 1:3) afforded 1.28 g of alcohol 165 (5.63 mmol, 98%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08242105B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-f572c0baee2042c88cf42ea0784e72f6 |
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| Source note | uspto-grants-2012_08 |
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