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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1644731생성일: 2026년 10월 27일

1,2-Dichloroethane → [6-Fluoro-4-(4-methanesulfonyl-benzoyl)-3-methyl-naphthalen-2-yl]-acetic acid methyl ester

https://huagongshe.com/reaction/1644731

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DichloroethaneHCID 11—
반응물Ethyl AcetateHCID 8857—
반응물Methyl pent-3-ynoateHCID 13378967—
반응물4-Fluoro-2-(4-methanesulfonyl-phenylethynyl)-benzaldehydeHCID 59350830—
촉매Gold tribromideHCID 82525—
용매HexaneHCID 8058—
생성물[6-Fluoro-4-(4-methanesulfonyl-benzoyl)-3-methyl-naphthalen-2-yl]-acetic acid methyl esterHCID 593508023.1%

반응 단계

To a mixture of 4-fluoro-2-(4-methanesulfonyl-phenylethynyl)-benzaldehyde (example 2-1, 3rd step) (2.02 g, 6.68 mmol) and pent-3-ynoic acid methyl ester (3.03 g, 26.8 mmol) in 1,2-dichloroethane (40 mL), was added gold(III) bromide (0.264 g, 1.18 mmol). The resulting mixture was heated at 80° C. for 2 hours before additional gold(III) bromide (0.125 g, 0.59 mmol) was added. Another portion of gold(III) bromide (0.125 g, 0.59 mmol) was added after 2 more hours. After a total of 6 hours of heating, the reaction mixture was cooled to room temperature, and the solvent was removed to afford a brown oil. Flash chromatography (Aspire FlashReady™, 50 μm, 30% ethyl acetate in hexane) gave [6-fluoro-4-(4-methanesulfonyl-benzoyl)-3-methyl-naphthalen-2-yl]-acetic acid methyl ester (87 mg, 3.1%). HRMS (ESI+) cald. for C22H19FO5S [(M+Na)+] 437.0829, obsd. 437.0827.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08124629B2
출처 데이터셋uspto-grants-2012_02
ORD IDord-c959dbfcb8bc4d81aa034a9c6ecddd3f
출처 메모uspto-grants-2012_02