反応式
[NH2:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][C:10]=2[NH2:12])[CH:5]=[CH:4][CH:3]=1.[F:13][C:14]([F:29])([O:19][C:20]1[CH:28]=[CH:27][C:23]([C:24]([Cl:26])=O)=[CH:22][CH:21]=1)[C:15]([F:18])([F:17])[F:16]>>[ClH:26].[F:13][C:14]([F:29])([O:19][C:20]1[CH:28]=[CH:27][C:23]([C:24]2[NH:1][C:2]3[CH:3]=[CH:4][CH:5]=[C:6]4[C:11]=3[C:10]([N:12]=2)=[CH:9][CH:8]=[CH:7]4)=[CH:22][CH:21]=1)[C:15]([F:16])([F:18])[F:17]参加物
3
実験手順
1,8-Diaminonaphthalene (1.04 grams; 0.00656 mole) and p-pentafluoroethoxybenzoyl chloride (1.8 grams; 0.00656 mole) were reacted in the procedures of Example 3, yielding 2.25 grams of product (82.7% yield), m.p., 240° C. (dec.), mass spectrum m/e 378.
出典と根拠
- ORDレコード
- ord-5d5a9964617249ab90e294e713446b26
- 出典データセット
- uspto-grants-1981_10
- 特許番号
- US04294964
関連ノート
読み込み中…