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Names | |
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IUPAC name
Allylmagnesium bromide
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Systematic IUPAC name
Prop-2-enylmagnesium bromide | |
Identifiers | |
3D model (
JSmol)
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ChemSpider | |
ECHA InfoCard | 100.015.497 |
PubChem
CID
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CompTox Dashboard (
EPA)
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Properties | |
C3H5BrMg | |
Molar mass | 145.282 g·mol−1 |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Allylmagnesium bromide is a Grignard reagent used for introducing the allyl group. It is commonly available as a solution in diethyl ether. It may be synthesized by treatment of magnesium with allyl bromide while maintaining the reaction temperature below 0 °C to suppress formation of hexadiene. [1] Allyl chloride can also be used in place of the bromide to give allylmagnesium chloride. [2] These reagents are used to prepare metal allyl complexes.
![]() | |
Names | |
---|---|
IUPAC name
Allylmagnesium bromide
| |
Systematic IUPAC name
Prop-2-enylmagnesium bromide | |
Identifiers | |
3D model (
JSmol)
|
|
ChemSpider | |
ECHA InfoCard | 100.015.497 |
PubChem
CID
|
|
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C3H5BrMg | |
Molar mass | 145.282 g·mol−1 |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Allylmagnesium bromide is a Grignard reagent used for introducing the allyl group. It is commonly available as a solution in diethyl ether. It may be synthesized by treatment of magnesium with allyl bromide while maintaining the reaction temperature below 0 °C to suppress formation of hexadiene. [1] Allyl chloride can also be used in place of the bromide to give allylmagnesium chloride. [2] These reagents are used to prepare metal allyl complexes.