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HRID 50468作成日:2026年10月24日

Acetic Acid → Ethyl 3-[[[3-(1,1,2,2-tetrafluoroethoxy)phenyl]methyl]amino]benzoate

https://huagongshe.com/ja/reaction/50468

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1,1-DichloroethaneHCID 6365—
反応物Ethyl 3-aminobenzoateHCID 11400—
反応物Benzaldehyde, 3-(1,1,2,2-tetrafluoroethoxy)-HCID 118803—
反応物Sodium triacetoxyborohydrideHCID 5049666—
生成物Ethyl 3-[[[3-(1,1,2,2-tetrafluoroethoxy)phenyl]methyl]amino]benzoateHCID 2350605299.9%

反応手順

EX-456A) Ethyl 3-aminobenzoate (6.75 mL, 0.045 mol) and 3-(1,1,2,2-tetrafluoro-ethoxy)benzaldehyde (10 g, 45 mmol) were dissolved in 100 mL. of dichloroethane and acetic acid (2.7 mL, 47 mmol), then solid NaBH(OAc)3 (14.3 g, 67 mmol) was added. The mixture was stirred at room temperature for 3 hours, then quenched with aqueous sodium bicarbonate and extracted with dichloromethane. The organic layer was washed with brine, then dried over MgSO4, and evaporated to give 16.7 g (98%) of the desired ethyl 3-[[[3-(1,1,2,2-tetrafluoroethoxy)phenyl]methyl]amino]benzoate product as a yellow oil. 1H NMR (CDCl3) δ 1.3 (t, 3H), 4.3 (q, 2H), 4.5 (s, 2H), 6.5 (tt, 1H), 6.9 (d, 1H), 7.1-7.4 (m, 7H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06710089B2
出典データセットuspto-grants-2004_03
ORD IDord-36cec2421c9946a5ae83edbbd1f2758d
出典メモuspto-grants-2004_03