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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1792969Generated: November 3, 2026

Water → 5-Benzo[b]thiophen-2-yl-2,4-dimethoxy-benzaldehyde

https://huagongshe.com/reaction/1792969

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzo(B)Thiophene-2-Boronic AcidHCID 2359—
ReactantSodium CarbonateHCID 10340—
Reactant5-Bromo-2,4-dimethoxybenzaldehydeHCID 668346—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
Product5-Benzo[b]thiophen-2-yl-2,4-dimethoxy-benzaldehydeHCID 1611591683%

Reaction Steps

Ex-6A: 5-Bromo-2,4-dimethoxybenzaldehyde (4.9 g, 20.0 mmol) was dissolved in ethylene glycol dimethyl ether (50 mL). Tetrakis(triphenylphosphine)palladium(0) (2.32 g, 2 mmol) was added, and the mixture was stirred at room temperature under nitrogen for 5 min. Benzo[b]thiophene-2-boronic acid (4.27 g, 24 mmol) and sodium carbonate solution (2 M, 20 mL) were added. The mixture was stirred at reflux under nitrogen for 24 hours. Upon cooling to room temperature, it was poured into water and extracted with ethyl acetate. The organic phase was dried over sodium sulfate and evaporated. Silica gel chromatography (hexane/ethyl acetate 2:1 then 1:1) gave 4.75 g (83%) of the desired 5-(benzo[b]thien-2-yl)-2,4-dimethoxybenzaldehyde.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07078431B2
Source datasetuspto-grants-2006_07
ORD IDord-099c434db9f545c5b23d9e1b226a3eb0
Source noteuspto-grants-2006_07