HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1756340Generated: October 29, 2026
Tetrabutylammonium Fluoride → HCID 19966471, compound
https://huagongshe.com/reaction/1756340
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 86748884 | HCID 86748884 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19966471 | HCID 19966471 | 59.3% |
Reaction Steps
914 mg of tetrabutylammonium fluoride is added to a solution of 500 mg of (5RS)-5-acetoxy-5-{3-[(1E,3E)-(5RS)-5-acetoxy-1,3-tridecadienyl]-phenyl}-pentan-1-ol-tert-butyldimethylsilylether in 28 ml of tetrahydrofuran at 0° C., stirred for 30 minutes at 0° C. and for 4.5 hours at 24° C. Then, it is diluted with ether, washed with brine, dried on sodium sulfate and concentrated by evaporation in a vacuum. The residue is chromatographed on silica gel. With hexane/0-20% ethyl acetate, 193 mg of (5RS)-5-acetoxy-5-{3-{(1E,3E)-(5RS)-5-acetoxy-1,3-tridecadienyl}-phenyl}-pentan-1-ol is obtained as colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05440044 |
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| Source dataset | uspto-grants-1995_08 |
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| ORD ID | ord-47c5067a23bd4c739078bf144ff38c9f |
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| Source note | uspto-grants-1995_08 |
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