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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1505290Generated: October 26, 2026

Tetrabutylammonium Fluoride → HCID 86638860, compound

https://huagongshe.com/reaction/1505290

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant(S,E)-Benzyl 8-(tert-butyldiphenylsilyloxy)-2-methyloct-5-en-4-ylcarbamateHCID 86638859—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86638860HCID 86638860—

Reaction Steps

To a solution of the TBDPS-protected alcohol 8b (584 mg, 1.10 mmol, crude) in dry THF (9 mL) at 0° C. was added TBAF (1.0M/THF, 1.38 mL, 1.38 mmol), and the reaction mixture was allowed to warm to rt while stirring under argon for 3.5 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 194 mg (60%, 2 steps) of the title compound as a colorless oil. [α]D23-6.4 (c 1.0, DCM); 1H NMR (300 MHz, CDCl3) δ 7.20-7.40 (m, 5 H), 5.65-5.49 (m, 1 H), 5.44 (dd, 1 H, J=15.3, 6.6 Hz), 5.09 (s, 2 H), 4.67 (bs, 1 H), 4.16 (m, 1 H), 3.63 (bs, 2 H), 2.28 (q, 2 H, J=6.0 Hz), 1.82 (bs, 1 H), 1.65 (m, 1 H), 1.40-1.25 (m, 2 H), 0.80-1.00 (m, 6 H); HRMS (E81) m/z calcd for C17H23NO3Na 314.1732. found 314.1739.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216976B2
Source datasetuspto-grants-2015_12
ORD IDord-ac0361d09a2d46339e272bc72b1771f7
Source noteuspto-grants-2015_12