HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 887115Generated: October 28, 2026
Tetrabutylammonium Fluoride → HCID 57907411, compound
https://huagongshe.com/reaction/887115
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 87174988 | HCID 87174988 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57907411 | HCID 57907411 | 100% |
Reaction Steps
To a stirred solution of 77.0 g, (236 mmol) of (5Z)-5-[(tert-butoxycarbonyl)hydrazono]-7-(trimethylsilyl)hept-6-ynoic acid from step B above in 500 mL of THF was added 350 mL (350 mmol) of a 1.0 M solution of tetrabutylammonium fluoride in THF over 30 min. The resulting mixture was stirred at ambient temperature for 48 h and then evaporated to dryness in vacuo. The residue was diluted with 1 L of a 5% aqueous acetic acid solution and the aqueous phase extracted with ethyl acetate (3×350 mL). The combined organic layers were washed with water (2×100 mL), and brine (150 mL), dried over magnesium sulfate, filtered and evaporated to dryness in vacuo. The crude residue was purified by silica gel chromatography eluting with 3% acetic acid and 35% ethyl acetate in hexanes mixture to afford the title compound as yellow oil (60 g, quantitative yield). LC-MS: m/z (ES) 255 (MH)−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08247415B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-1f304b9555314d7d988912797a55ac1c |
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| Source note | uspto-grants-2012_08 |
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