Styrene → HCID 86751228, compound
Reaction equation
[Mg:1].[CH2:2]1[CH2:6]O[CH2:4][CH2:3]1.[CH2:7]=[CH:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1.C=CC=C>CCCCCC>[CH2:6]=[CH:2][CH:3]=[CH2:4].[CH2:7]=[CH:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1.[Mg:1]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
To each of two 10-ounce crown-capped beverage bottles was charged 1 gram of 50-mesh magnesium shavings (41 mM), followed by 30 ml. of THF and 10 ml. styrene (86.5 mM in THF). To one of the bottles (#1), 38.4 grams of 23.6% 1,3-butadiene in hexane (167 mM) were charged. To the other bottle (#2), 43.5 grams of 23.6% 1,3-butadiene in hexane (140 mM) were charged. Bottle #1 was placed in an ultrasound bath to activate the magnesium metal. Bottle #2 was placed in a 65° C. water bath. After three days at 65° C., most, but not all, of the magnesium in bottle #1 had reacted. The reaction in bottle #2 took longer and some magnesium was still present after seven days at 65° C.
Workup
- customBottle #1 was placed in an ultrasound bath
- customwas placed in a 65° C.
- customThe reaction in bottle #2
Sources & evidence
- ORD record
- ord-208c04daffab4a008aab218ce643cc8f
- Source dataset
- uspto-grants-1997_10
- Patent number
- US05677399
Reaction notes
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