HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 874796Generated: October 30, 2026
Tetrabutylammonium Fluoride → HCID 56619794, compound
https://huagongshe.com/reaction/874796
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 86677602 | HCID 86677602 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 56619794 | HCID 56619794 | — |
Reaction Steps
To a stirred and ice-cold solution of 3-[2-(tert-butyldimethylsilanyloxy)-ethyl]-1-vinylpyrrolidin-2-one (TBSE-VP) (269 mg; 1.0 mmol) in dry tetrahydrofuran (10 mL) was dropwise added a 1.0 M solution of tetrabutylammonium fluoride (2.0 mL; 2.0 mmol; 2.0 equiv.) under an argon atmosphere. Upon completion of the addition the reaction mixture was left stirring at 0° C. for 5 min, allowed to warm to ambient temperature over 5 min and left stirring for another 40 min. The reaction mixture was partitioned between water (5 mL) and ethyl acetate (10 mL) and the aqueous phase was extracted with ethyl acetate (3×5 mL). The combined organic extracts were dried over MgSO4 and concentrated under reduced pressure. Column chromatography (ethyl acetate) afforded the target compound (135 mg; 0.87 mmol; 87%) as a pale yellow liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08980956B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-4cff1e84761340819fdba9f73753cc01 |
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| Source note | uspto-grants-2015_03 |
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