戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1017031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/1017031

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

EX-654B) The 3-t-butoxybenzaldehyde (0.585 g, 3.27 mmol) 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US06476057B1
出典データセットuspto-grants-2002_11
ORD IDord-da176ce507d548d489cd13a5020de814
出典メモuspto-grants-2002_11