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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 632655Generated: October 30, 2026

Dichloromethane → HCID 86730673, compound

https://huagongshe.com/reaction/632655

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantAcetic acid, 2-(triphenylphosphoranylidene)-, methyl esterHCID 17453—
Reactant5-((6-Methoxy-2-(4-methoxyphenyl)benzo[b]thiophen-3-yl)oxy)picolinaldehydeHCID 86730672—
ProductHCID 86730673HCID 8673067332%

Reaction Steps

To a solution of 5-((6-methoxy-2-(4-methoxyphenyl)benzo[b]thiophen-3-yl)oxy)picolinaldehyde (0.265 g, 0.68 mmol) in DCM (3.38 mL) at 0° C. was added methyl 2-(triphenylphosphoranylidene)acetate (0.543 g, 1.63 mmol) and the reaction was stirred at room temperature for 18 h. Upon completion the mixture was concentrated in vacuo to afford crude material which was purified by column chromatography (SiO2, 0-25% EtOAc/heptanes) to afford (E)-methyl 3-(5-((6-methoxy-2-(4-methoxyphenyl)benzo[b]thiophen-3-yl)oxy)pyridin-2-yl)acrylate (96 mg, 0.22 mmol, 32% yield). 1H NMR (400 MHz, CDCl3) δ ppm=3.70-3.75 (m, 6H), 3.79-3.83 (m, 3 H), 6.70 (d, J=15.66 Hz, 1 H), 6.77-6.88 (m, 3 H), 7.02 (dd, J=8.59, 3.03 Hz, 1 H), 7.17 (s, 1 H), 7.18-7.22 (m, 2 H), 7.48-7.59 (m, 3 H), 8.42 (d, J=2.53 Hz, 1 H). LC/MS (m/z, MH+): 448.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321746B2
Source datasetuspto-grants-2016_04
ORD IDord-842b15bde121478da673379b2bbada07
Source noteuspto-grants-2016_04