Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1354001Generated: November 4, 2026

Tetrahydrofuran → cis-Stilbene

https://huagongshe.com/reaction/1354001

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant3-Fluoro-4,5-dimethoxybenzaldehydeHCID 603447—
ReactantPhosphoniumHCID 5460504—
ReactantButyllithiumHCID 178418339—
SolventEthyl acetate hexaneHCID 21226206—
Productcis-StilbeneHCID 535678534%

Reaction Steps

To a mixture of phosphonium salt 6 (4.7 g, 6.5 mmol) and tetrahydrofuran (25 ml, cooled to −78° C.) was added n-BuLi (2.6 mL, 2.5 M, 6.5 mmol, over 5 minutes), followed by stirring for one hour. Next, 3-fluoro-4,5-dimethoxybenzaldehyde (1g, 5.4 mmol) in tetrahydrofuran (10 ml) was added (dropwise) over 30 minutes. The mixture was allowed to warm to room temperature, and stirring continued for 16 hours. The reaction was terminated by the addition of water (50 mL), the product was extracted with ethyl acetate, solvents were removed in vacuo, and the residue (1:1 E/Z, 75% yield) obtained was subjected to flash chromatography on silica gel using hexane-ethyl acetate (9:1) as eluent to afford Z-stilbene 7a (1 g, 34%) as a clear oil; 1H-NMR (300 MHz, CDCl3) δ 1.07 (s, 9H), 3.46 (s, 3H), 3.65 (s, 3H), 3.90 (s, 3H), 6.24 (d, 1H, J=12 Hz), 6.33 (d, 1H, J=12 Hz), 6.56 (m, 2H), 6.72 (m, 3H), 7.35 (m, 6H), 7.70 (m, 4H); and 12C NMR (75 MHz, CDCl3) δ 19.75, 26.65, 55.07, 55.99, 61.43, 108.26, 108.28, 109.40, 109.55, 111.74, 120.83, 122.42, 127.36, 127.46, 127.48, 127.70, 129.37, 129.50, 129.63, 130.32, 132.59, 132.66, 133.57, 134.77, 135.27, 135.83, 135.95, 144.74, 149.88, 152.91, 152.95, 154.59, 156.53; HRMS (calcd for C33H36FO4Si) [M+H]+ 543.2368, found 543.2372.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07223747B2
Source datasetuspto-grants-2007_05
ORD IDord-99d0a2593bf14a38bb4813a235ca7f26
Source noteuspto-grants-2007_05