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HRID 48033作成日:2026年10月25日

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

https://huagongshe.com/reaction/48033

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Ethyl 3-aminobenzoateHCID 11400—
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) δ1.3 (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US06699898B2
出典データセットuspto-grants-2004_03
ORD IDord-e0481ebadd7d45a68043a6d4d2531157
出典メモuspto-grants-2004_03