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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386040Generated: November 1, 2026

Tetrahydrofuran → HCID 18615581, compound

https://huagongshe.com/reaction/1386040

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant6-Bromo-2H-1,3-benzodioxole-4-carbaldehydeHCID 12514097—
ReactantHCID 178418573HCID 178418573—
SolventButyl etherHCID 8909—
ProductHCID 18615581HCID 1861558165.4%

Reaction Conditions

Temperature25 °C

Reaction Steps

To 150 mL tetrahydrofuran, was added 6-bromo-benzo[1,3]dioxole-4-carbaldehyde (15 g, 65.4 mmol). To the solution was added a solution of methyl magnesium bromide (1.0 M) in di-n butyl ether (72 mL) followed by exotherm and solid formation. The mixture was stirred at 25° C. for 2.5 hours and evaporated in vacuo to a solid. The mixture was suspended in ethyl acetate washed with 1N citric acid, brine, and dried over anhydrous magnesium sulfate. The mixture was filtered and evaporated to an oil. The oil was induced to crystallize from ethyl acetate and hexane giving a white solid which was filtered and dried in vacuo giving a solid, 10.48 g, 65.4% yield. NMR spectra and elemental analysis were consistent with the structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265399B1
Source datasetuspto-grants-2001_07
ORD IDord-dc65bcf231e949b18390d190e6d7a246
Source noteuspto-grants-2001_07