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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222314Generated: October 31, 2026

6-Bromo-2-fluoro-3-methoxybenzaldehyde → 2-Fluoro-3-methoxy-6-vinylbenzaldehyde

https://huagongshe.com/reaction/222314

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Bromo-2-fluoro-3-methoxybenzaldehydeHCID 23157915—
ReactantPotassium vinyltrifluoroborateHCID 23679353—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
Solvent1-PropanolHCID 1031—
Product2-Fluoro-3-methoxy-6-vinylbenzaldehydeHCID 57722773—

Reaction Steps

To a stirred solution of 6-bromo-2-fluoro-3-methoxybenzaldehyde (13 g, 56 mmol) in nPrOH (200 mL) were added potassium vinyltrifluoroborate (7.9 g, 59 mmol), PdCl2(dppf) (0.91 g, 1.1 mmol), and TEA (7.8 mL, 56 mmol). The reaction mixture was purged with N2 for 10 min, heated to reflux for 3 h, cooled to room temperature, treated with water, and concentrated. The residue was extracted with EtOAc (×3). The combined organics were washed with brine, dried (Na2SO4), concentrated, and purified by flash chromatography to afford the title compound. 1H NMR (600 MHz, CDCl3) δ 10.53 (s, 1H); 7.43 (dd, 1H); 7.31 (d, 1H); 7.16 (t, 1H); 5.60 (d, 1H); 5.36 (d, 1H); 3.95 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207186B2
Source datasetuspto-grants-2012_06
ORD IDord-bd8e3e39fc5340a6bf66c7f53c006236
Source noteuspto-grants-2012_06