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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1424664생성일: 2026년 10월 23일

Methanol → Methyl 4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)-5-fluoropicolinate

https://huagongshe.com/ko/reaction/1424664

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물Sodium MethoxideHCID 10942334—
반응물Florpyrauxifen-benzylHCID 70495450—
용매WaterHCID 962—
생성물Methyl 4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)-5-fluoropicolinateHCID 57412076—

반응 단계

Benzyl 4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)-5-fluoropicolinate (3.00 g, 6.83 mmol) was added to CH3OH (35 mL). Sodium methoxide (25 wt % in CH3OH; 1.9 mL, 8.2 mmol) was added to the reaction mixture. and the reaction mixture was allowed to stir for 24 h. Water (50 mL) was added to the reaction mixture, and the mixture was concentrated under reduced pressure to remove most of the CH3OH. The mixture was extracted with EtOAc (2×40 mL), and the combined organic layers were washed with water (40 mL) and satd sodium chloride (40 mL). Concentration of the volatiles under reduced pressure provided methyl 4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)-5-fluoropicolinate as a pale yellow solid (2.04 g, 88% purity by LC area).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08927731B2
출처 데이터셋uspto-grants-2015_01
ORD IDord-aa1e933017a648e89a8e1de269a72982
출처 메모uspto-grants-2015_01