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HRID 48037作成日:2026年10月23日

Acetic Acid → N-(3-nitrophenyl)-3-(1,1,2,2-tetrafluoroethoxy)benzenemethanamine

https://huagongshe.com/ja/reaction/48037

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物3-NitroanilineHCID 7423—
反応物Benzaldehyde, 3-(1,1,2,2-tetrafluoroethoxy)-HCID 118803—
反応物Sodium triacetoxyborohydrideHCID 5049666—
溶媒1,1-DichloroethaneHCID 6365—
生成物N-(3-nitrophenyl)-3-(1,1,2,2-tetrafluoroethoxy)benzenemethanamineHCID 2350609370%

反応手順

Ex-528A) 3-nitroaniline (1.87 g, 13.51 mmol) and 3-(1,1,2,2-tetrafluoroethoxy)-benzaldehyde (3 g, 13.5 mmol) were dissolved in 25 mL of dichloroethane and acetic acid (0.85 mL, 14.9 mmol), then solid NaBH(OAc)3 (3.73 g, 17.6 mmol) was added. The mixture was stirred at room temperature for 48 hours, then quenched with aqueous saturated sodium bicarbonate and diluted with ethyl acetate. The organic layer was dried over MgSO4, and concentrated in vacuo. The crude product was purified by flash column chromatography on silica gel eluting with ethyl acetate:hexane 1:7 to give 3.25 g (70%) of the desired N-(3-nitrophenyl)-3-(1,1,2,2-tetrafluoroethoxy) benzenemethan-amine product as a brown oil. HRMS calcd. for C15H13F4N2O3: 345.0862 [M+H]+, found: 345.0864. 1H NMR (CDCl3) δ4.4 (s, 2H), 4.5 (s, 11H), 5.9 (tt, 1H), 6.9 (d, 1H), 7.1 (d, 1H), 7.2-7.3 (m, 3H), 7.4 (m, 2H), 7.5 (d, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06699898B2
出典データセットuspto-grants-2004_03
ORD IDord-1bc75ceba99841dabf8c86f8896091f2
出典メモuspto-grants-2004_03