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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 654947Generated: October 30, 2026

1,2-Dibromoethane → HCID 19885932, compound

https://huagongshe.com/reaction/654947

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DibromoethaneHCID 7839—
ReactantMagnesiumHCID 5462224—
Reactant5-(Trimethylsilyl)furan-3-carbaldehydeHCID 15663251—
ReactantHCID 21705970HCID 21705970—
ReactantHCID 178419678HCID 178419678—
SolventTetrahydrofuranHCID 8028—
ProductHCID 19885932HCID 19885932—

Reaction Steps

To a stirred solution of 8-(thiophene-2-yl)octyl magnesium bromide [0.62 mmol, prepared from 1-bromo-8-(thiophen-2-yl)octane; 0.170 g, 0.620 mmol and 1.24 mmol magnesium with a catalytic amount of 1,2 dibromoethane as initiator] in tetrahydrofuran (2 ml) at 0° under argon was added dropwise 5-trimethylsilyl-3-furaldehyde (0.104 g, 0.620 mmol) in tetrahydrofuran (3 ml). The solution was warmed to room temperature, stirred for one hour, quenched with saturated ammonium chloride solution and extracted into ethyl ether. The organic portion was washed with saturated sodium bicarbonate solution, water, saturated sodium chloride solution, dried over magnesium sulfate, filtered and concentrated to a yellow oil. Purification by flash chromatography (silica, 5 to 10% ethyl acetate/hexane) gave the desired alcohol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05134128
Source datasetuspto-grants-1992_07
ORD IDord-52607143f4244f858675f778ce1534f5
Source noteuspto-grants-1992_07