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Azobisisobutyronitrile → cis-5-Norbornene-endo-2,3-dicarboxylic Anhydride tert-butyl 5-Norbornene-2-carboxylate maleic Anhydride mono-methyl cis-5-Norbornene-endo-2,3-dicarboxylate 5-norbornene-2-carboxylic Acid

HRID 1611420
ノート
印刷プレビュー

反応式

HRID 1611420 の反応式
[C:1]1(=[O:7])[O:6][C:4](=[O:5])[CH:3]=[CH:2]1.[CH2:8]1[C@@H:12]2[CH:13]3[C:18](=[O:19])[O:17][C:15](=[O:16])[CH:14]3[C@H:9]1[CH:10]=[CH:11]2.[CH3:20][O:21][C:22]([CH:24]1[CH:28]([C:29]([OH:31])=[O:30])[CH:27]2[CH:32]=[CH:33][CH:25]1[CH2:26]2)=[O:23].[C:34]([O:38][C:39]([CH:41]1[CH2:46][CH:45]2[CH2:47][CH:42]1[CH:43]=[CH:44]2)=[O:40])([CH3:37])([CH3:36])[CH3:35].N(C(C)(C)C#N)=NC(C)(C)C#N>O1CCCC1>[CH2:8]1[C@@H:12]2[CH:13]3[C:18](=[O:19])[O:17][C:15](=[O:16])[CH:14]3[C@H:9]1[CH:10]=[CH:11]2.[CH:42]12[CH2:47][CH:45]([CH:44]=[CH:43]1)[CH2:46][CH:41]2[C:39]([O:38][C:34]([CH3:37])([CH3:36])[CH3:35])=[O:40].[C:4]1(=[O:5])[O:6][C:1](=[O:7])[CH:2]=[CH:3]1.[CH3:20][O:21][C:22]([CH:24]1[CH:28]([C:29]([OH:31])=[O:30])[CH:27]2[CH:32]=[CH:33][CH:25]1[CH2:26]2)=[O:23].[CH:9]12[CH2:8][CH:12]([CH:11]=[CH:10]1)[CH2:13][CH:14]2[C:15]([OH:17])=[O:16]
参加物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 6547AzobisisobutyronitrileHCID 7923Maleic AnhydrideHCID 984652-Methyl bicyclo(2.2.1)hept-5-ene-2,3-dicarboxylateHCID 9964188cis-5-Norbornene-endo-2,3-dicarboxylic anhydrideHCID 15607334Bicyclo[2.2.1]hept-5-ene-2-carboxylic acid, 1,1-dimethylethyl ester

生成物 1

HCID 131723902
cis-5-Norbornene-endo-2,3-dicarboxylic Anhydride tert-butyl 5-Norbornene-2-carboxylate maleic Anhydride mono-methyl cis-5-Norbornene-endo-2,3-dicarboxylate 5-norbornene-2-carboxylic Acid

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

Maleic anhydride (1.0 mole), cis-5-norbornene-endo-2,3-dicarboxylic anhydride (0.2 mole), mono-methyl cis-5-norbornene-endo-2,3-dicarboxylate (0.15 mole) and tert-butyl-5-norbornene-2-carboxylate (0.65 mole) are dissolved in tetrahydrofuran. Then, 0.5 to 10 g of AIBN (azobisisobutyronitrile) as a polymerization initiator is added thereto, and the resultant mixture is reacted at about 60-70° C. for 4 to 24 hours under nitrogen or argon atmosphere. The polymer thus obtained is precipitated from ethyl ether or hexane, and dried to obtain the compound represented by the following Chemical Formula 101.

後処理

  1. customThe polymer thus obtained
  2. customis precipitated from ethyl ether or hexane
  3. customdried
  4. customto obtain the compound

出典と根拠

ORDレコード
ord-c1bc7c4a979845838d0d71f4f84a1cf1
出典データセット
uspto-grants-2006_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06987155B2

反応ノート

読み込み中…

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