Ethyl Bromide → HCID 178418443, compound
Reaction equation
[Mg:1].C([Br:4])C.[CH3:5][C:6]#[CH:7]>O1CCCC1>[CH2:6]([Mg:1][Br:4])[CH3:7].[C:7]([Mg:1][Br:4])#[C:6][CH3:5]Participants
Reactant 3
Product 2
Reagents, catalysts & solvents 1
Procedure
Ethylmagnesium bromide was prepared in a similar manner to Example 1 from 12 g (0.5 mole) of metallic magnesium in 250 ml of tetrahydrofuran and 5.4 g (0.05 mole) of ethyl bromide instead of 54 g (0.5 mole). Then, 10 ml of a tetrahydrofuran solution containing 2 g (0.05 mole) of methylacetylene were added dropwise to the reaction mixture kept at 40° to 50° C. to form 1-propynylmagnesium bromide. Further, 57.2 g (0.4 mole) of chloromethyl dimethyl chlorosilane were added dropwise into the reaction mixture kept at 50° to 70° C. over a period of 4 hours followed by aging at 66° C. for 2 hours. The reaction mixture was subjected to hydrolysis with a saturated aqueous solution of ammonium chloride and the organic solution taken from the mixture by phase separation was distilled under reduced pressure to remove the solvent leaving 31 g of a viscous liquid residue as the reaction product.
Workup
- additionwere added dropwise to the reaction mixture
- customkept at 40° to 50° C.
Sources & evidence
- ORD record
- ord-198c357085b444928b9698118ab36a14
- Source dataset
- uspto-grants-1985_09
- Patent number
- US04539417
Reaction notes
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