HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2246723Generated: November 2, 2026
Tetrabutylammonium Fluoride → HCID 68528780, compound
https://huagongshe.com/reaction/2246723
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 68525183 | HCID 68525183 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68528780 | HCID 68528780 | 84% |
Reaction Steps
1′-[3-{[tert-butyl(dimethyl)silyl]oxy}-1-(3-fluorophenyl) propyl]spiro-[cyclohexane-1,3′-indol]-2′(1′H)-one (0.85 g, 1.82 mmol) was dissolved in tetrahydrofuran and tetrabutyl ammonium fluoride (1.0 M in THF, 3.64 mL, 3.64 mmol) was added and the mixture was stirred for 1 hour. Reaction was quenched with saturated aqueous ammonium chloride then saturated sodium bicarbonate was added, diluted with ether, washed with water, and saturated brine. The organic layer was separated, dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo. The crude product was purified via Isco chromatography (Redisep, silica, gradient 0-100% ethyl acetate in hexane) to afford 0.54 g (84%) racemic 1′-[1-(3-fluorophenyl)-3-hydroxypropyl]spiro[cyclohexane-1,3′-indol]-2′(1′H)-one that was resolved by chiral HPLC
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07687529B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-fb6141471e36425990fa4b0a2b986ea0 |
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| Source note | uspto-grants-2010_03 |
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