HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016160Generated: November 1, 2026
Tetrabutylammonium Fluoride → HCID 57888692, compound
https://huagongshe.com/reaction/1016160
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 86614928 | HCID 86614928 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57888692 | HCID 57888692 | 80% |
Reaction Steps
A solution of 2-(trimethylsilyl)ethyl (2R)-1-(8-(4-chlorophenyl)-8-hydroxy-5-azaspiro[2.5]octan-5-yl)-3-methyl-1-oxobutan-2-ylcarbamate (754 mg, 1.567 mmol) in THF (10 mL) was treated with TBAF (1.0 M in THF) (6.27 mL, 6.27 mmol), and the mixture was stirred overnight at room temperature. The reaction mixture was concentrated in-vacuo, and the residue was partitioned between EtOAc and saturated sodium bicarbonate. The layers were separated, and the organic phase was washed 2× with saturate sodium bicarbonate, once with water, and once with brine. The combined aqueous phases were extracted once with ethyl acetate, and the combined organic phases were washed with water and brine, then dried over sodium sulfate and concentrated in-vacuo. The residue was taken up in acetonitrile (100 mL), and washed 3× with 20 mL of hexanes. The acetonitrile phase was concentrated in-vacuo to yield the title compound (420 mg, 1.247 mmol, 80% yield) as a colorless glass. MS (ESI+)=337.4, (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07985861B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-0ef015a0da0b4858a255e7cf9a768e7f |
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| Source note | uspto-grants-2011_07 |
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