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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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Styrene → 1,2-Diethenylbenzene

HRID 745829
ノート
印刷プレビュー

反応式

HRID 745829 の反応式
[Li].C([Li])(CC)C.C=CC=C.C=CC1C=CC=CC=1.C1(N[C:26]2[CH:35]=[CH:34][C:33]3[C:28](=[CH:29][CH:30]=[CH:31][CH:32]=3)[CH:27]=2)C=CC=CC=1>CCCCCC.O>[CH:27]([C:28]1[CH:29]=[CH:30][CH:31]=[CH:32][C:33]=1[CH:34]=[CH2:35])=[CH2:26]
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 5

HCID 7501Styrene2 回HCID 78451,3-Butadiene2 回HCID 8679N-phenyl-2-naphthylamineHCID 3028194LithiumHCID 178418400CID 53628100

生成物 1

HCID 666661,2-Diethenylbenzene

試薬・触媒・溶媒 2

HCID 962
Water
溶媒
HCID 8058Hexane溶媒3 回

実験手順

Still further, in a nitrogen atmosphere, 213 m mole as active lithium of sec-butyllithium was added to a 15 wt.% n-hexane solution of 9.5 kg of a monomer mixture comprising 1,3-butadiene and styrene in a weight ratio of 40:60, and the mixture was polymerized at 60° C. for 4 hours. After more than 99% of the monomers had been polymerized, the resulting active copolymer solution was further mixed with a 20 wt.% n-hexane solution of 19.0 kg of a monomer mixture comprising 1,3-butadiene and styrene in a weight ratio of 70:30, and the mixture was polymerized first at 70° C. for 4 hours and then at 85° C. for one hour. After substantially all of the monomer mixture had been copolymerized, the resulting final copolymer was inactivated by addition of a small amount of water. To the copolymer solution, 285 g of phenyl-β-naphthylamine was added. Thereafter, n-hexane was volatilized to obtain a non-divinylbenzene-incorporated thermoplastic elastomer in accordance with the present process (sample H), and the physical properties thereof were measured.

後処理

  1. customthe mixture was polymerized at 60° C. for 4 hours
  2. customthe mixture was polymerized first at 70° C. for 4 hours
  3. customcopolymerized

出典と根拠

ORDレコード
ord-1079989e1dc54d729c3caecedd402bc7
出典データセット
uspto-grants-1986_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04600749

反応ノート

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