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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 61811생성일: 2026년 10월 24일

Hydrochloric Acid → 4-(3-Bromo-4-methoxy-phenyl)-4-methyl-3-oxo-pentanoic acid ethyl ester

https://huagongshe.com/ko/reaction/61811

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Methanesulfonic AcidHCID 6395—
반응물1-Acetoxy-2-bromoethaneHCID 13564—
반응물2-(3-Bromo-4-methoxyphenyl)-2-methylpropionitrileHCID 11368810—
촉매ZincHCID 23994—
용매TetrahydrofuranHCID 8028—
생성물4-(3-Bromo-4-methoxy-phenyl)-4-methyl-3-oxo-pentanoic acid ethyl esterHCID 6683466572%

반응 조건

온도80 °C

반응 단계

To the THF suspension of zinc (5.72 g, 2 eq.), methanesulfonic acid (25.6 μl, 0.01 eq.) was added, and then stirred at 80° C. for 10 min. Then, the THF solution of 2-(3-bromo-4-methoxy-phenyl)-2-methyl-propionitrile (10 g, 39.35 mmol) was added, followed by addition of bromoethyl acetate (11.07 ml, 1.6 eq.) over 1 hr. The mixture was further stirred for 30 min. To the reaction solution, 4 M hydrochloric acid was added, and stirred at room temperature overnight. After extraction with ethyl acetate, the organic layer was washed with brine and dried over sodium sulfate. The drying agent was removed by filtration and the residues obtained after concentration under reduced pressure were purified by silica gel column chromatography (ethyl acetate/hexane) to obtain the title compound (orange oily substance, 9.74 g, 72%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09440922B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-e3caf457cc424c3a82933351d7c7f175
출처 메모uspto-grants-2016_09