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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 226137생성일: 2026년 10월 26일

1-Naphthalenemethanamine → 3-{3-[(Naphthalen-1-ylmethyl)-sulfamoyl]-phenyl}-acrylic acid methyl ester

https://huagongshe.com/reaction/226137

반응식

참여 물질

역할이름HCID투입량
반응물1-NaphthalenemethanamineHCID 8355—
반응물Sodium BicarbonateHCID 516892—
반응물3-(3-Chlorosulfonylphenyl)acrylic acid methyl esterHCID 73708742—
용매WaterHCID 962—
용매1,4-DioxaneHCID 31275—
생성물3-{3-[(Naphthalen-1-ylmethyl)-sulfamoyl]-phenyl}-acrylic acid methyl esterHCID 6701954076%

반응 단계

A solution of 3-(3-chlorosulfonylphenyl)acrylic acid methyl ester (3) (0.4 g, 1.53 mmol) in dioxane (5 ml) was added to a mixture of 1-naphthalenemethylamine (0.24 g, 1.53 mmol) in dioxane (1 ml) and NaHCO3 (0.25 g, 3.06 mmol) in water (3 ml), and the resultant solution was stirred at room temperature until the completion of the reaction (control by TLC). The reaction mixture was evaporated and the residue was partitioned between ethyl acetate and 2N HCl. The organic layer was washed successively with water, saturated NaCl1 and dried (Na2SO4). The solvent was removed and the residue was chromatographed on silica gel with petroleum ether-ethyl acetate (2:1, v/v) as eluent. The obtained product was washed with diethyl ether to give the title compound (0.44 g, 76%) as a white solid. 1H NMR (DMSO-d6, HMDSO), δ: 3.74 (3H, s); 4.47 (2H, d, J=6.0 Hz); 6.69 (1H, d, J=16.0 Hz); 7.32-8.32 (13H, m).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07557140B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-ce6780fef75c4923a829dacb12c62c8f
출처 메모uspto-grants-2009_07