HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1823124Generated: October 31, 2026
Tetrabutylammonium Fluoride → HCID 24824075, compound
https://huagongshe.com/reaction/1823124
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 24823941 | HCID 24823941 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 24824075 | HCID 24824075 | 73.4% |
Reaction Steps
To a solution of [4-[2-[N-benzyl-N-[(2R)-2-[[tert-butyl (dimethyl) silyl]oxy]-2-(3-chlorophenyl) ethyl]amino]-ethyl]phenyl][4-[[tert-butyl(dimethyl)silyl]oxy]phenyl]-methanol (1.1 g) in tetrahydrofuran (15 ml) was added 1M tetrabutylammonium fluoride in tetrahydrofuran (5.0 ml) at 0° C., and the mixture was stirred at room temperature for 24 hours under nitrogen. The mixture was partitioned between ethyl acetate and water. The organic layer was separated, washed with water and brine, dried over magnesium sulfate and evaporated under reduced pressure. The residue was purified by column chromatography on silica gel (hexane/ethyl acetate=2/1) to give 4-[[4-[2-[N-benzyl-N-[(2R)-2-(3-chlorophenyl)-2-hydroxyethyl]amino]ethyl]-phenyl](hydroxy)methyl]phenol (550 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07037938B2 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-f7fc24cc007941a7a63e83164745c21a |
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| Source note | uspto-grants-2006_05 |
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