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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1892038생성일: 2026년 10월 26일

Hydrochloric Acid → (3-Bromo-quinolin-6-yloxy)-methylsulfanyl-acetic acid

https://huagongshe.com/reaction/1892038

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium HydroxideHCID 14798—
반응물(3-Bromo-quinolin-6-yloxy)-methylsulfanyl-acetic acid methyl esterHCID 59565456—
용매EthanolHCID 702—
용매WaterHCID 962—
생성물(3-Bromo-quinolin-6-yloxy)-methylsulfanyl-acetic acidHCID 6671784498%

반응 단계

To a solution of (3-bromo-quinolin-6-yloxy)-methylsulfanyl-acetic acid methyl ester (20 g) from Step 1, Stage 1 above in ethanol (150 ml) at R.T. a 2 M solution of sodium hydroxide in water (35.06 ml) was added. The reaction mixture was stirred at R.T. for 2 hours. The reaction mixture was poured into ice-could water (200 ml) and acidified with a 2 M solution of hydrochloric acid in water (35.06 ml). The precipitate was filtered off and washed with water to give (3-Bromo-quinolin-6-yloxy)-methylsulfanyl-acetic acid as yellowish solid (18.79 g). 1H NMR (CDCl3) δ ppm: 13.50 (1H, s br); 8.83 (1H, d); 8.59 (1H, d); 7.99 (1H, d); 7.57 (1H, dd); 7.50 (1H, d); 6.09 (1H, s); 2.17 (3H, s).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08507509B2
출처 데이터셋uspto-grants-2013_08
ORD IDord-2983e6841bea48128c45d4494996bc6f
출처 메모uspto-grants-2013_08