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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1451313Generated: October 28, 2026

Hexane → HCID 10464590, compound

https://huagongshe.com/reaction/1451313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 86749955HCID 86749955—
ReactantButyllithiumHCID 178418339—
CatalystMethyltriphenyliphosphonium bromideHCID 74505—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
ProductHCID 10464590HCID 1046459086%

Reaction Steps

To a suspension of methyltriphenylphosphonium bromide (145 g; 0.405 mol, dried at 60° C.) in 1 L of ether was added at -20° C. n-butyllithium in hexane (2.5M, 162 ml; 0.405 mol) and the mixture was allowed to stir at room temperature for 1 h. To the above mixture was added 60 g (0.37 mol) of 1,1-di(3-furyl)ketone in 450 ml of DME/THF/DMPU (2:2:0.5) in 10 minutes and the mixture was stirred at room temperature for 1 h.. To the above reaction mixture was added saturated ammonium chloride solution (250 ml), and the mixture was diluted with 500 ml of water. The organic layer was separated, washed with water (2×500 ml), dried, and concentrated in vacuo. The residue was purified by chromatography on silica (hexane, then 10% ether/hexane) to afford 51 g (86%) of 1,1-di(3-furyl)ethylene (Formula III: R2 =R3 =H; R4 =R5 =3-furanyl). This product was further distilled (b.p. 60°-63° C./0.01 mm).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05604224
Source datasetuspto-grants-1997_02
ORD IDord-3281f59934dd4f8297985e25f050a3db
Source noteuspto-grants-1997_02