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HRID 1296850생성일: 2026년 10월 25일

4-Chloronaphthylamine → (2-(4-(((4-Chloronaphthyl)amino)methyl)phenoxy)ethyl)diethylamine

https://huagongshe.com/reaction/1296850

반응식

참여 물질

역할이름HCID투입량
반응물4-ChloronaphthylamineHCID 78408—
반응물4-(2-(Diethylamino)-Ethoxy)-BenzaldehydeHCID 411674—
반응물Sodium borohydrideHCID 4311764—
촉매p-Toluenesulfonic acid monohydrateHCID 521998—
용매MethanolHCID 887—
용매TolueneHCID 1140—
생성물(2-(4-(((4-Chloronaphthyl)amino)methyl)phenoxy)ethyl)diethylamineHCID 235143812,089.2%

반응 단계

A stirred solution of 0.2 gram (0.0001 mole) of 4-(2-(diethylamino)ethoxy)benzaldehyde (prepared in the manner of Step A, Example 3), 0.22 gram (0.0001 mole) of 1-amino-4-chloronaphthalene (available from Aldrich Chemical Company), and one drop of p-toluenesulfonic acid monohydrate (available from Aldrich Chemical Company) in 5 mL of toluene was heated at reflux for ten hours. At the conclusion of this period, the reaction mixture was concentrated under reduced pressure, yielding a residue. The residue was taken up in 5 mL of methanol and about 0.2 grams (0.004 mole) of sodium borohydride was added. The resulting mixture was stirred at ambient temperature for about 18 hours. After this time, the mixture was quenched with water and extracted with several portions of diethyl ether. The extracts were combined, dried with sodium sulfate and filtered. The filtrate was concentrated under reduced pressure, yielding 0.8 gram of Compound 84. The NMR spectrum was consistent with the proposed structure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07247756B2
출처 데이터셋uspto-grants-2007_07
ORD IDord-75cb64f9bedf4ead93f4feb3873e1e84
출처 메모uspto-grants-2007_07