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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337594Generated: October 26, 2026

Tetrahydrofuran → 3-Bromo-5-(3-methoxypropyl)benzaldehyde

https://huagongshe.com/reaction/337594

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant1-Propene, 3-methoxy-HCID 69392—
Reactant3,5-DibromobenzaldehydeHCID 622077—
ReactantSodium MethoxideHCID 10942334—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventWaterHCID 962—
Product3-Bromo-5-(3-methoxypropyl)benzaldehydeHCID 86651671—

Reaction Steps

To a THF solution (0.3 M) of allyl methyl ether (3.1 eq.) at RT was added borane-methyl sulfide complex (1.0 eq.). The solution was stirred at RT for 30 min. To this solution was then added sequentially 3,5-dibromobenzaldehyde (1.0 eq.), Pd(dppf)Cl2 (0.025 eq.) and solid sodium methoxide (1.5 eq.). The resulting mixture was heated to reflux for 15 h. The cooled reaction mixture was diluted with water and extracted with ether. The combined organic extracts were dried over MgSO4, filtered and the filtrate concentrated in vacuo. Purification of the crude product thus obtained by way of flash chromatography (SiO2, 5:95 (v/v) EtOAc:Hex→7:3 (v/v) EtOAc:Hex) afforded the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889714B2
Source datasetuspto-grants-2014_11
ORD IDord-c80d014c2c464857ad4045dce4aa9992
Source noteuspto-grants-2014_11