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HRID 50468생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물1,1-DichloroethaneHCID 6365—
반응물Ethyl 3-aminobenzoateHCID 11400—
반응물Benzaldehyde, 3-(1,1,2,2-tetrafluoroethoxy)-HCID 118803—
반응물Sodium triacetoxyborohydrideHCID 5049666—
생성물Ethyl 3-[[[3-(1,1,2,2-tetrafluoroethoxy)phenyl]methyl]amino]benzoateHCID 2350605299.9%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06710089B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-36cec2421c9946a5ae83edbbd1f2758d
출처 메모uspto-grants-2004_03