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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1681237Generated: October 29, 2026

1,3-Butadiene → HCID 101926094, compound

https://huagongshe.com/reaction/1681237

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-ButadieneHCID 7845—
ReactantTetrahydrofuranHCID 8028—
ReactantDichloro(phenyl)silaneHCID 74207—
ReactantMagnesiumHCID 5462224—
SolventEthylene GlycolHCID 174—
SolventDiethyl EtherHCID 3283—
ProductHCID 101926094HCID 10192609419%

Reaction Steps

In a 500 mL two neck rb flask equipped with a reflux condenser, a Teflon covered magnetic stirring bar and a rubber septum was placed magnesium powder (9.6 g, 0.4 mol), phenyldichlorosilane (35.4g, 0.2 mol) and THF (300 mL). The reflux condenser was connected to a refrigeration unit. Ethylene glycol cooled to -20° C. was circulated through the reflux condenser. 1,3-Butadiene (15.1 g, 0.28 mol) was condensed at -78° C. into a volumetric flask which was sealed with a rubber septum. The 1,3-butadiene was transferred into the reaction via a cannula. The reaction mixture was stirred at rt for 24 h. Ether (2×100 mL) was added. The organic solution was decanted from the magnesium chloride salts. These were transferred to a sintered glass funnel and were washed with ether (100 mL). The combined organic solution was washed with water (2×50 mL), dried over anhydrous magnesium sulfate, filtered and the volatile solvents removed by evaporation under reduced pressure. The residue was purified by distillation through a 10 cm vacuum jacketed Vigreux column. A fraction, bp 87°/5 mm, 6.0 g, 19% yield, was collected.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05169916
Source datasetuspto-grants-1992_12
ORD IDord-089654f2d0fa4f77bbf85e08c9f9386c
Source noteuspto-grants-1992_12