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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1193025Generated: October 26, 2026

Furfural → ([4-Bromo-2,6-dimethylphenyl]furan-2-yl)methanol

https://huagongshe.com/reaction/1193025

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFurfuralHCID 7362—
ReactantAmmonium ChlorideHCID 25517—
Reactant5-Bromo-2-iodo-1,3-dimethylbenzeneHCID 2735573—
ReactantHCID 178418918HCID 178418918—
SolventTetrahydrofuranHCID 8028—
Product([4-Bromo-2,6-dimethylphenyl]furan-2-yl)methanolHCID 6670961182.5%

Reaction Conditions

Temperature-78 °C

Reaction Steps

4-Bromo-2,6-dimethyl-1-iodobenzene (5 g, 16 mmol) is dissolved in dry tetrahydrofuran (20 ml) and cooled to −78° C. under an atmosphere of dry nitrogen. Isopropylmagnesium chloride (2M solution in tetrahydrofuran, 10 ml, 20 mmol) is added dropwise with vigorous stirring over 30 minutes. When the addition is complete, the reaction is allowed to warm to room temperature and is stirred for 30 minutes at room temperature. The reaction mixture is cooled to −78° C. and a solution of 2-furaldehyde (2.4 g, 25 mmol) in dry tetrahydrofuran (10 ml) is added dropwise over 30 minutes. Once the addition is complete, the mixture is allowed to warm to room temperature and stirring continued for 2 hours. A solution of saturated aqueous ammonium chloride (30 ml). is added, and the mixture is extracted with dichloromethane (3×25 ml). The organic extracts are combined, washed with brine, dried over anhydrous magnesium sulfate, filtered and the filtrate is evaporated under reduced pressure. The residue is purified by column chromatography on silica gel to give ([4-bromo-2,6-dimethylphenyl]furan-2-yl)methanol (3.71 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680339B2
Source datasetuspto-grants-2014_03
ORD IDord-0be7fb479df94a41b7e743df13130fc0
Source noteuspto-grants-2014_03