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1,3-Benzenedimethanamine → Isophthalonitrile

HRID 607336
ノート
印刷プレビュー

反応式

HRID 607336 の反応式
[C:1]1([CH2:9][NH2:10])[CH:6]=[CH:5][CH:4]=[C:3]([CH2:7][NH2:8])[CH:2]=1>C1(C)C=CC=C(C)C=1>[C:9](#[N:10])[C:1]1[CH:6]=[CH:5][CH:4]=[C:3]([C:7]#[N:8])[CH:2]=1
参加物実験手順出典と根拠反応ノート

参加物

3

反応物 1

HCID 151331,3-Benzenedimethanamine

生成物 1

HCID 12276Isophthalonitrile

試薬・触媒・溶媒 1

HCID 7929M-Xylene溶媒2 回

実験手順

Patent Document 1 discloses a method of producing m-xylylenediamine from m-xylene. In the proposed method, isophthalonitrile produced by the ammoxidation of m-xylene is extracted into an organic solvent. Then, high-boiling point impurities are separated out in the first distillation step and the organic solvent is separated out in the second distillation step. Then, isophthalonitrile is taken out of the bottom of apparatus. The obtained purified isophthalonitrile is then hydrogenated after the addition of a specific solvent and liquid ammonia. This method requires increased costs for constructing production facilities because of its large number of steps. In addition, the method requires two distillation steps before the hydrogenation and further requires another distillation step for purification after the hydrogenation step. Therefore, a great quantity of energy for distillation should be consumed.

出典と根拠

ORDレコード
ord-200d897774664b2482fc06458a2b0287
出典データセット
uspto-grants-2011_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07915452B2

反応ノート

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