Dichlorodimethylsilane → 2-Methylbuta-1,3-diene;styrene

HRID 1908940Notes

Reaction equation

HRID 1908940 reaction equation
CN(CCN(C)C)C.[CH2:9]=[CH:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1.C([Li])CCC.[CH2:22]=[CH:23][C:24](=[CH2:26])[CH3:25].C[Si](C)(Cl)Cl.Cl[Si](Cl)(Cl)Cl>C1CCCCC1>[CH2:9]=[CH:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1.[CH2:22]=[CH:23][C:24](=[CH2:25])[CH3:26].[CH2:9]=[CH:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1.[CH2:9]=[CH:10][C:11](=[CH2:12])[CH3:16].[CH2:9]=[CH:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1

Participants

9

Reactant 6

HCID 6398DichlorodimethylsilaneHCID 6557Isoprene3×HCID 7501Styrene2×HCID 8037N,N,N',N'-TetramethylethylenediamineHCID 24816Silicon tetrachlorideHCID 178418339Butyllithium

Product 2

HCID 1599892-Methylbuta-1,3-diene;styreneHCID 19842620HCID 19842620, compound

Reagents, catalysts & solvents 1

HCID 8078CyclohexaneSolvent

Conditions

Temperature
40 °C

Procedure

In a pressure resistant reactor, 23.3 kg of cyclohexane, 5.00 millimoles of TMEDA, and 1.90 kg of styrene were added, and while the mixture was stirred at 40° C., 166.7 millimoles of n-butyllithium was added thereto. While the temperature was elevated to 50° C., polymerization was carried out for one hour. The polymerization conversion ratio for styrene was 100%. Subsequently, while the temperature was controlled to be maintained at 50° C. to 60° C., 5.20 kg of isoprene was continuously added to the reactor over one hour. After completion of the addition of isoprene, polymerization was carried out for another one hour. The polymerization conversion ratio for isoprene was 100%. Thereafter, 50.0 millimoles of dimethyldichlorosilane and 12.5 millimoles of tetrachlorosilane were added to the reactor as coupling agents, and a coupling reaction was carried out for 2 hours. Thus, a styrene-isoprene-styrene block copolymer and a branched styrene-isoprene block copolymer were formed. Subsequently, 333.4 millimoles of methanol was added to the reaction liquid which was believed to have a styrene-isoprene block copolymer having an active terminal remaining therein. The resulting mixture was thoroughly mixed, and thereby the active terminal was deactivated. A portion of the reaction liquid thus obtained was taken out, and the same measurements as in Example 1 were made. These values are presented in Table 2. The subsequent operation was carried out in the same manner as in Example 1, and a block copolymer composition of Comparative Example 1 was collected. The block copolymer composition was fabricated into pellets and was thereby formed into a film of Comparative Example 1. Measurements were made for this film. The results are presented in Table 2.

Workup

  1. customwas elevated to 50° C.
  2. custompolymerization
  3. temperatureto be maintained at 50° C. to 60° C.
  4. waitwas carried out for another one hour
  5. customa coupling reaction
  6. waitwas carried out for 2 hours

Sources & evidence

ORD record
ord-35b849c2630041e79bad5b9516b4e9f5
Source dataset
uspto-grants-2013_12
Patent number
US08598271B2

Reaction notes

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