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HRID 1840050作成日:2026年10月27日

Acetic Acid → N-(3-phenoxyphenyl)[[3-(1,1-dimethylethoxy)phenyl]methyl]amine

https://huagongshe.com/reaction/1840050

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-PhenoxyanilineHCID 77135—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物3-Tert-butoxybenzaldehydeHCID 15712224—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
溶媒Ethyl AcetateHCID 8857—
生成物N-(3-phenoxyphenyl)[[3-(1,1-dimethylethoxy)phenyl]methyl]amineHCID 1093694841.6%

反応手順

The 3-t-butoxybenzaldehyde (0.585 g, 3.27 nmmol) product from EX-654A and 3-phenoxyaniline (0.595 g, 3.21 mmol) were combined in 50 mL of THF, then solid NaBH(OAc)3 (0.860 g, 4.06 mmol) was added, and the mixture was stirred until uniform. Acetic acid (0.2 g, 3.33 mmol) was added, and the mixture was stirred at room temperature for 4 h, then quenched with 5% aq. NaHCO3. The aqueous layer was separated and extracted twice with ether. The combined ether layers were washed with water and brine, dried over MgSO4, filtered, and evaporated to give 1.29 g (115%) of crude product as a brown oil. Chromatography on silica gel eluting with 0-10% ethyl acetate in hexane gave 464 mg (40%) of the desired N-(3-phenoxyphenyl)[[3-(1,1-dimethyl-ethoxy)phenyl]methyl]amine product as a colorless oil, pure by TLC. MS m/z=347 [M+].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06677375B2
出典データセットuspto-grants-2004_01
ORD IDord-b5155c5a982d49159cef8a01837a222e
出典メモuspto-grants-2004_01