HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 70492Generated: October 29, 2026
Tetrabutylammonium Fluoride → HCID 86638864, compound
https://huagongshe.com/reaction/70492
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 86638861 | HCID 86638861 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86638864 | HCID 86638864 | 92.4% |
Reaction Steps
To a solution of the TBDPS-protected alcohol 11b (320 mg, 0.588 mmol) in dry THF (5 mL) at 0° C. was added TBAF (1.0M/THF, 0.74 mL, 0.735 mmol), and the reaction mixture was allowed to warm to rt while stirring under argon for 7 h, then quenched with sat. aq. NH4Cl and diluted with EtOAc. The aqueous phase was separated and extracted with EtOAc. The combined organic layers were washed with brine, dried (Na2SO4), filtered and concentrated in vacuo. Flash chromatography (SiO2, 5:5, hexanes/EtOAc) afforded 166 mg (92%) of the title compound as a colorless oil. [α]D23−21.6 (c 1.0, DCM); 1H NMR (300 MHz, CDCl3) δ 7.42-7.28 (m, 5H), 5.10 (m, 2H), 4.76 (appbd, 1H, J=5.7 Hz), 3.63 (bs, 2H), 3.04 (m, 1H), 2.12-1.98 (bs, 1H), 1.83-1.62 (m, 2H), 1.42 (t, 2H, J=7.0 Hz), 1.16-0.95 (m, 2H), 0.90 (appt, 6H, J=7.0 Hz), 0.53 (sept, 1H, J=4.3 Hz), 0.42 (dt, 1H, J=8.4, 4.5 Hz), 0.34 (dt, 1H, J=8.4, 5.0 Hz); HRMS (ESI) m/z calcd for C18H27NO3Na 328.1889; found 328.1860.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08822541B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-0d46852b4f9c46649b96847b46168583 |
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| Source note | uspto-grants-2014_09 |
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