1,3-Bis(isocyanatomethyl)benzene → Hexamethylene diisocyanate
反応式
[CH:1]1[CH:6]=[C:5](CN=C=O)[CH:4]=[C:3]([CH2:11][N:12]=[C:13]=[O:14])C=1.C1(CN=C=O)C(C[N:22]=[C:23]=[O:24])=CC=CC=1>>[CH2:1]([N:22]=[C:23]=[O:24])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:11][N:12]=[C:13]=[O:14]参加物
3
実験手順
The same isocyanuration reaction as in Production Example 1 was carried out except that 3,290 g of hexamethylene diisocyanate and 210 g of "Takenate 500" (xylylene diisocyanate produced by Takeda Chemical Industry Co., Ltd.) were used instead of 3,500 g of hexamethylene diisocyanate, and the amount of the isocyanuration catalyst used in production Example 1 was changed to 4.7 g. There was obtained 4,219 g of the reaction mixture containing the deactivated catalyst.
後処理
- customThe same isocyanuration reaction as in Production Example 1
出典と根拠
- ORDレコード
- ord-b586495e75b64103b8ef0e456075ea8c
- 出典データセット
- uspto-grants-1991_10
- 特許番号
- US05055514
反応ノート
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