HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1098163Generated: November 3, 2026
Tetrabutylammonium Fluoride → HCID 59279518, compound
https://huagongshe.com/reaction/1098163
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 66813452 | HCID 66813452 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59279518 | HCID 59279518 | 59% |
Reaction Steps
Tetrabutylammonium fluoride (1M in THF) (2071 μl, 2.07 mmol) was added to (S)-methyl 2-(tert-butyldiphenylsilyloxy)-4-(methylsulfonyl)butanoate (Intermediate AA3) (450 mg, 1.04 mmol) in THF (3106 μl) under nitrogen. The resulting mixture was stirred at ambient temperature for 2 hours. The reaction mixture was quenched with saturated NH4Cl (10 mL), extracted with Et2O (3×15 mL). The combined organic layers were back washed with water (10 mL), dried (MgSO4) and evaporated. The crude product was purified by flash silica chromatography, eluting with 0 to 100% ethyl acetate in isohexane to afford the product (120 mg, 59%). 1H NMR (400 MHz, CDCl3) δ 2.10-2.20 (1H, m), 2.38-2.46 (1H, m), 2.94 (4H, m), 3.10-3.24 (2H, m), 3.84 (3H, s), 4.34 (1H, q), 7.26 (3H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08143263B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-9112af410c0943949d87d22f4d38828f |
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| Source note | uspto-grants-2012_03 |
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