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HRID 2372016作成日:2026年10月25日

p-Toluenesulfonic acid → 2,3-Dihydro-1,3-dimethyl-2-dodecylperimidine

https://huagongshe.com/reaction/2372016

反応式

関与物質

役割名称HCID仕込み量
反応物p-Toluenesulfonic acidHCID 6101—
反応物Sodium HydroxideHCID 14798—
反応物TridecanalHCID 25311—
反応物N,N'-Dimethyl-1,8-naphthalenediamineHCID 140748—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物2,3-Dihydro-1,3-dimethyl-2-dodecylperimidineHCID 15404100—

反応手順

A mixture of N,N'-dimethyl-1,8-naphthalene diamine (prepared in Example 1) (0.50 g, 2.7 mmol, 186), tridecanal (0.56 g, 2.85 mmol. 197), p-toluenesulfonic acid (5 mg), and tetrahydrofuran (5 ml) was prepared and stirred at room temperature for 15 minutes. The mixture was basified with 25% sodium hydroxide (1.0 ml), diluted with water (20 ml) and extracted with ether (100 ml). The extract was dried over potassium carbonate, concentrated to give 2,3-dihydro-1,3-dimethyl-2-dodecyl perimidine as a solid: mp 30°-32° C.; NMR (CDCl3) 7.13(m, 4H), 6.32(d, 2H), 4.27(t, 1H), 3.02(s, 6H), 1.7-1.1(m, 22H), 0.85(t, 3H); IR (neat) 1595 cm-1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05097029
出典データセットuspto-grants-1992_03
ORD IDord-94ad1b5147d04401a56bb19c28001f31
出典メモuspto-grants-1992_03