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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 481097생성일: 2026년 10월 25일

Ethyl bromoacetate → Acetic acid, (p-tolylsulfonyl)-, ethyl ester

https://huagongshe.com/reaction/481097

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl bromoacetateHCID 7748—
반응물Potassium CarbonateHCID 11430—
반응물6-Methoxy-3-nitro-2-(toluene-4-sulfonylmethyl)-pyridineHCID 13626514—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물Acetic acid, (p-tolylsulfonyl)-, ethyl esterHCID 76102—

반응 조건

온도50 °C

반응 단계

A mixture of 5.0 g (15.5 mmol) of 6-methoxy-3-nitro-2-(toluene-4-sulfonyl methyl)-pyridine and 1.8 mL (16 mmol) of ethyl bromoacetate is dissolved in 20 mL of DMF. To this solution is added 4.4 g (32 mmol) of K2CO3 and the reaction mixture is heated to 50° C. for 18 hours. The reaction mixture is cooled to room temperature and diluted with 300 mL of water. The mixture is extracted with ethyl acetate. The ethyl acetate extracts are dried (Na2SO4) and evaporated to yield 7.2 grams of 6-methoxy-3-nitro-pyridin-2-yl]-[toluene-4-sulfonyl]-acetic acid ethyl ester. 1H NMR (CDCl3) δ8.30 (d, 1H), 7.60 (d, 2H), 7.30 (d, 2H), 6.80 (d, 1H), 6.30 (m, 1H), 4.0 (q, 2H), 3.80 (s, 3H), 3.60 (m, 1H), 3.10 (m, 1H), 2.40 (s, 3H), 1.10 (t, 3H). Mass spectrum: m/e=409.0 (p+1). TLC (7/3: hexanes/ethyl acetate) Rf=0.5.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06653471B2
출처 데이터셋uspto-grants-2003_11
ORD IDord-97ab4a5da0c1460097e7333967f6bea6
출처 메모uspto-grants-2003_11