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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 602751생성일: 2026년 10월 26일

Methyl chloroacetate → (Naphthalene-1-sulfonyl)-acetic acid methyl ester

https://huagongshe.com/reaction/602751

반응식

참여 물질

역할이름HCID투입량
반응물Methyl chloroacetateHCID 7295—
반응물Potassium CarbonateHCID 11430—
반응물1-NaphthalenethiolHCID 68259—
반응물Potassium hydroxy sulfiteHCID 23707502—
용매AcetoneHCID 180—
생성물(Naphthalene-1-sulfonyl)-acetic acid methyl esterHCID 6726733655.4%

반응 조건

온도0 °C

반응 단계

To a stirred suspension of 3.1 g (0.019 mol) of naphthalene-1-thiol and 2.94 g (0.021 mol, 1.1 eq) of K2CO3 in 100 mL of propan-2-one cooled at 0° C., 3.15 g (0.029 mol, 1.5 eq) of chloro-acetic acid methyl ester were added in one portion. The ice bath was removed and the reaction mixture was stirred an additional 4 hours. The reaction was filtered, the solvent evaporated and the resulting residue was taken up in 100 mL of MeOH. 14.3 g (0.023 mol, 1.2 eq) of oxone (potassium peroxymonosulfate) were added and the reaction mixture was stirred over night at RT. The salts were filtered off, the solvent evaporated and the residue purified by column chromatography on silica gel with heptane/EtOAc (from 4:1 to 1:2) to afford 2.78 g (55%) of (naphthalene-1-sulfonyl)-acetic acid methyl ester as a light yellow oil, MS: 265 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07906546B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-8b117963bb6648eeb711e6a3174dc962
출처 메모uspto-grants-2011_03