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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1451312Generated: November 1, 2026

3-Bromofuran → HCID 19047515, compound

https://huagongshe.com/reaction/1451312

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromofuranHCID 89164—
ReactantHCID 10487090HCID 10487090—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
ProductHCID 19047515HCID 1904751578.4%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of n-butyllithium (2.5M, 28 ml, 0.07 mol) in 150 ml of ether at -78° C. was added a solution of 3-bromofuran (10 g, 0.0628 mol) in 30 ml of ether over a 20 min period and the mixture was stirred at -78° C. for 20 min. To the above mixture was added 3-(N-methyl-N-methoxycarbamoyl)furan (9.16 g, 0.059 mol) in 30 ml of ether over a 15 min period and the mixture was stirred at room temperature for 1/2 h. The reaction mixture was quenched with 200 ml of ammonium chloride solution, 500 ml of methylene chloride was added and the mixture was stirred. The organic layer was dried over sodium sulfate, concentrated in vacuo, and the residue was triturated in 100 ml of hexane/t-butylmethylether (9:1). The solid product was filtered and washed with t-butylmethylether to afford 7.5 g (78.3%) of di-(3-furyl)ketone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05604224
Source datasetuspto-grants-1997_02
ORD IDord-97d85dccf2e34f988de982dddefaec95
Source noteuspto-grants-1997_02