反応 #4155973
関連文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-db0ca1b7e921436ba5f4a58e0588df9e表示可能な構造データがありません
CC(C)(C1=CC=CC=C1)Cl製品情報
2-chloropropan-2-ylbenzene (CAS 934-53-2) product identity, structure identifiers and related reaction data for chemical intermediate research and sourcing review.
想定用途
専門的研究・工業用途限定
データベース ID 70281
安全上の注意
For professional research and industrial use only. Review the supplier safety data sheet before handling.
合成データ
12 反応 · 12 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-db0ca1b7e921436ba5f4a58e0588df9e反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-4ed919ac3fa742ab994d646492587449反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-4ebc0ebe76c94a9c88f964ad7a45452c反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-448259f3f7a1468eb88e364fd99a2182反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-e051f3b2cea046889c50b4462852d483反応条件: temp:-70.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: In a 2 L reaction vessel equipped with a stirrer, 589 mL of methylcyclohexane (dried over molecular sieves), 613 mL of n-butyl chloride (dried over molecular sieves) and 0.550 g of cumyl chloride were charged. After cooling the reaction vessel to −70° C., 0.35 mL of a-picoline (2-methylpyridine) and 179 mL of isobutylene were added. Further, 9.4 mL of titanium tetrachloride was added to start polymerization, and then the solution was reacted for 2.0 hours while being stirred at −70° C. Next, 59 mL of styrene was added into the reaction vessel and the reaction was continued for 60 minutes, and then the reaction was terminated by adding a large amount of methanol. After removing the solvent and the like from the reaction solution, a polymer was dissolved in toluene and washed twice with water. This toluene solution was added to the methanol mixture, thereby precipitating a polymer, and the resultant polymer was dried at 60° C. for 24 hours to obtain a styrene-isobutylene diblock copolymer. In a 2 L reaction vessel equipped with a stirrer polymerization the solution was reacted for 2.0 hours the reaction was terminated by adding a large amount of methanol After removing the solvent the like from the reaction solution, a polymer was dissolved in toluene washed twice with water This toluene solution was added to the methanol mixture precipitating a polymer the resultant polymer was dried at 60° C. for 24 hours
ソース ID: ord-d5f2995ff3554ab88448916b8364c38c反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-db0ca1b7e921436ba5f4a58e0588df9e反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-4ed919ac3fa742ab994d646492587449反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-4ed919ac3fa742ab994d646492587449反応条件: temp:-70.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: In a 2 L reaction vessel equipped with a stirrer, 589 mL of methylcyclohexane (dried over molecular sieves), 613 mL of n-butyl chloride (dried over molecular sieves) and 0.550 g of cumyl chloride were charged. After cooling the reaction vessel to −70° C., 0.35 mL of α-picoline (2-methylpyridine) and 179 mL of isobutylene were added. Further, 9.4 mL of titanium tetrachloride was added to start polymerization, and then the solution was reacted for 2.0 hours while being stirred at −0.70° C. Next, 59 mL of styrene was added into the reaction vessel and the reaction was continued for 60 minutes, and then the reaction was terminated by adding a large amount of methanol. After removing the solvent and the like from the reaction solution, a polymer was dissolved in toluene and washed twice with water. This toluene solution was added to the methanol mixture, thereby precipitating a polymer, and the resultant polymer was dried at 60° C. for 24 hours to obtain a styrene-isobutylene diblock copolymer. In a 2 L reaction vessel equipped with a stirrer polymerization the solution was reacted for 2.0 hours the reaction was terminated by adding a large amount of methanol After removing the solvent the like from the reaction solution, a polymer was dissolved in toluene washed twice with water This toluene solution was added to the methanol mixture precipitating a polymer the resultant polymer was dried at 60° C. for 24 hours
ソース ID: ord-f2758879c9dc4ea1bb005ab901567eac反応条件: temp:-70.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: In a 2 L reaction vessel equipped with a stirrer, 589 mL of methylcyclohexane (dried over molecular sieves), 613 mL of n-butyl chloride (dried over molecular sieves) and 0.550 g of cumyl chloride were charged. After cooling the reaction vessel to −70° C., 0.35 mL of α-picoline (2-methylpyridine) and 179 mL of isobutylene were added. Further, 9.4 mL of titanium tetrachloride was added to start polymerization, and then the solution was reacted for 2.0 hours while being stirred at −0.70° C. Next, 59 mL of styrene was added into the reaction vessel and the reaction was continued for 60 minutes, and then the reaction was terminated by adding a large amount of methanol. After removing the solvent and the like from the reaction solution, a polymer was dissolved in toluene and washed twice with water. This toluene solution was added to the methanol mixture, thereby precipitating a polymer, and the resultant polymer was dried at 60° C. for 24 hours to obtain a styrene-isobutylene diblock copolymer. In a 2 L reaction vessel equipped with a stirrer polymerization the solution was reacted for 2.0 hours the reaction was terminated by adding a large amount of methanol After removing the solvent the like from the reaction solution, a polymer was dissolved in toluene washed twice with water This toluene solution was added to the methanol mixture precipitating a polymer the resultant polymer was dried at 60° C. for 24 hours
ソース ID: ord-f2758879c9dc4ea1bb005ab901567eac反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 4.644 g (0.03 mol) of α,α-dimethylbenzyl chloride and 2.373 g (0.03 mol) of pyridine were reacted in 40 ml of methanol at 40° C. for 3 days. After the reaction, the solvent was evaporated in vacuo and ether-water was added to the residue to extract unreacted reactants in the etherial layer. To the aqueous layer was added 7.7 g (0.03 mol) of sodium hexafluoroantimonate. The resulting crystals were suction filtered, washed and dried to give the title compound. After the reaction the solvent was evaporated in vacuo and ether-water was added to the residue to extract unreacted reactants in the etherial layer filtered washed dried
ソース ID: ord-1b22a44aef0d43dda0d4773ae0c0d2eaPubChem References
化合物の公開データベース記録に掲載された情報源です。
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