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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1613115Generated: November 1, 2026

Homoallyl bromide → Bisbutenyl mercury

https://huagongshe.com/reaction/1613115

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHomoallyl bromideHCID 21241—
ReactantMagnesiumHCID 5462224—
ReactantBis(3-butenyl)mercuryHCID 12533408—
ReactantHCID 178418797HCID 178418797—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductBisbutenyl mercuryHCID 8674567760%

Reaction Steps

Preparation of bis(3-butenyl)mercury: To a solution of 3-butenylmagnesium bromide, prepared from 25 g of 1-bromo-3-butene (187 mmole) and 5 g of magnesium (208 mmole) in 40 mL of tetrahydrofuran, was added dropwise, at 50° C. with stirring, a solution of 25.2 g of mercuric chloride (93 mmole) in tetrahydrofuran. After stirring for 2 hours at 60° C., the reaction mixture was hydrolyzed with water at 0°-5° C. Organic layer was separated from aqueous layer; the product was distilled to give bisbutenyl mercury in 60% yield. The yield of the desired product was confirmed by gas chromatography (GC) and 1H NMR.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05192616
Source datasetuspto-grants-1993_03
ORD IDord-c734b09e9cf34009a087b33304658c33
Source noteuspto-grants-1993_03