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Styrene → Benzene, ethenyl-, polymer with 1,3-butadiene

HRID 1959484
ノート
印刷プレビュー

反応式

HRID 1959484 の反応式
[CH2:1]=[CH:2][C:3]1C=CC=C[CH:4]=1.C=CC=C.O1CCCC1CCC.C([Li])CCC.C(C1C=C2C3=C4C(C=CC=C4C=C2)=CC=C3C=1C)[CH:27]=[CH:28][C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1.CCOCC>CCCCCC>[CH2:1]=[CH:2][CH:3]=[CH2:4].[CH2:27]=[CH:28][C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 5

HCID 7501StyreneHCID 78451,3-ButadieneHCID 5512402-PropyltetrahydrofuranHCID 86620807HCID 86620807、化合物HCID 178418339Butyllithium

生成物 1

HCID 62697Benzene, ethenyl-, polymer with 1,3-butadiene

試薬・触媒・溶媒 1

HCID 8058
Hexane
溶媒

反応条件

温度
23 °C

実験手順

To a 10 oz. nitrogen purged bottle, hexane (20 mL), styrene (1 gr, 30% in hexane), butadiene (5 gr, 20% in hexane), oligomeric oxolanyl propane (OOPs) (0.03 mL, 1.6M solution) and butyl lithium (0.1 mL, 1.54M) would be added. The bottle would be placed into 80° C. water bath for 10 minutes. After cooling to 23° C., a charge of cinnamyl-1-methylpyrene ether (10 mL, 0.14M in cyclohexane) would be added into the bottle. After continual cooling for 5 minutes, a charge of DVB (0.5 mL) would be added to the mixture. The reaction would proceed for 1 hour, and then would be terminated by adding isopropanol 0.1 mL).

後処理

  1. customwould be placed into 80° C.
  2. customfor 10 minutes
  3. additionwould be added into the bottle
  4. temperatureAfter continual cooling for 5 minutes
  5. additiona charge of DVB (0.5 mL)
  6. additionwould be added to the mixture
  7. customThe reaction
  8. customwould be terminated
  9. additionby adding isopropanol 0.1 mL)

出典と根拠

ORDレコード
ord-edcf516085b0469db1f2e5614c4442ef
出典データセット
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08410225B2

反応ノート

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