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HRID 513320作成日:2026年10月25日

Tetrahydrofuran → 5-(6-bromonaphthalen-2-yl)-N1,N3-bis(4-methoxyphenyl)-N1,N3-diphenylbenzene-1,3-Diamine

https://huagongshe.com/reaction/513320

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物Potassium CarbonateHCID 11430—
反応物2,6-DibromonaphthaleneHCID 640591—
反応物N1,N3-bis(4-methoxyphenyl)-N1,N3-diphenyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene-1,3-diamineHCID 68193967—
触媒HCID 178418397HCID 178418397—
溶媒WaterHCID 962—
生成物5-(6-bromonaphthalen-2-yl)-N1,N3-bis(4-methoxyphenyl)-N1,N3-diphenylbenzene-1,3-DiamineHCID 68193747—

反応手順

13.42 g of a product (yield: 66%) was obtained in the same manner as described in the synthesis method of intermediate 2-3 except that N1,N3-bis(4-methoxyphenyl)-N1,N3-diphenyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene-1,3-diamine (17.76 g, 30 mmol), 2,6-dibromonaphthalene (9.44 g, 33 mmol), Pd(PPh3)4 (1.04 g, 0.9 mmol), K2CO3 (12.44 g, 90 mmol), THF (90 mL), and water (45 mL) were used.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09102616B2
出典データセットuspto-grants-2015_08
ORD IDord-17559f20e43e4b8f8c2a43fb252975b4
出典メモuspto-grants-2015_08