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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 386384생성일: 2026년 10월 25일

Hydrochloric Acid → Ethyl 2-(naphthalen-1-yl)-3-oxobutanoate

https://huagongshe.com/reaction/386384

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Acetic AnhydrideHCID 7918—
반응물alpha-Naphthaleneacetic acid, ethyl esterHCID 62428—
반응물Lithium HexamethyldisilazideHCID 2733832—
용매TetrahydrofuranHCID 8028—
생성물Ethyl 2-(naphthalen-1-yl)-3-oxobutanoateHCID 54265160—

반응 조건

온도-78 °C

반응 단계

To a solution of ethyl 2-(naphthalen-1-yl)acetate (1 g, 4.7 mmol) in tetrahydrofuran (20 mL) at −78° C. was added LiHMDS (1M THF, 9.4 mL, 9.4 mmol) and the reaction mixture stirred at −78° C. for 1 hour. Acetic anhydride was then added (0.54 mL, 5.64 mmol) dropwise and the reaction allowed to warm to room temperature and stirred for 30 minutes. Aqueous HCl solution (1N, 25 mL) was added to the reaction mixture and then extracted with ethyl acetate, dried over sodium sulfate and concentrated to give compound ethyl 2-(naphthalen-1-yl)-3-oxobutanoate as a light yellow oil, that was used in the next step without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08372807B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-900794aa6d0849628b825587973780c5
출처 메모uspto-grants-2013_02