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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 629841생성일: 2026년 10월 26일

Hydrochloric Acid → 873806-20-3

https://huagongshe.com/reaction/629841

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 5017741—
반응물ButyllithiumHCID 178418339—
반응물HCID 178462446HCID 178462446—
용매TetrahydrofuranHCID 8028—
생성물873806-20-3HCID 12171955—

반응 조건

온도-78 °C

반응 단계

To a stirred solution of Ia (7.0 g, 50 mmol) in dry THF (25 mL) at −78° C. was added n-BuLi (1.6 M in n-hexane, 62.5 mL, 100 mmol). After being stirred for 1 hour at −78° C., the reaction mixture was warmed to room temperature and stirred for 1 hour at that temperature. Another flask was charged with 2-isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (7.8 mL, 38 mmol) in dry THF (50 mL) under argon atmosphere, and the reaction mixture was cooled to −78° C. The lithium acetylide from the first flask, which was cooled to −78° C., was slowly added to the second by a double-ended needle. The mixture was stirred at −78° C. for 2 hours, after which anhydrous HCl (100 mmol) was added. Then, reaction mixture was warmed to room temperature. After removal of the precipitated LiCl by filtration and removal of solvents under reduced pressure, the residue was purified by distillation (113-115° C./7 mbar) to afford IIIa (5.9 g, 80%) as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09315525B2
출처 데이터셋uspto-grants-2016_04
ORD IDord-d0388a5d128947039f58c65e1a47e386
출처 메모uspto-grants-2016_04