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HRID 601456생성일: 2026년 10월 25일

2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane → 4,4,5,5-Tetramethyl-2-(4-octylphenyl)-1,3,2-dioxaborolane

https://huagongshe.com/reaction/601456

반응식

참여 물질

역할이름HCID투입량
반응물2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 5017741—
반응물1-Iodo-4-octylbenzeneHCID 11594836—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물4,4,5,5-Tetramethyl-2-(4-octylphenyl)-1,3,2-dioxaborolaneHCID 58823386—

반응 조건

온도-78 °C

반응 단계

n-BuLi (16.6 mL, 1.6 M in hexanes) was added over 10 minutes to a solution of 1-iodo-4-octylbenzene from Part A (6.9 g, 21.8 mmol) in dry THF (100 mL) at −78° C. under a nitrogen atmosphere. The mixture was stirred for another 10 minutes at −78° C. 2-Isopropoxy-4,4,5,5-tetramethyl[1,3,2]dioxaborolane (6.21 mL, 30.4 mmol) was subsequently added dropwise to the mixture and stirring was continued at room temperature overnight. The reaction was then quenched with distilled water, and THF was removed under vacuum. The product was then extracted into diethyl ether and the organic layer was washed with brine, dried over MgSO4, filtered and evaporated in vacuo to give 6.38 g of 4,4,5,5-tetramethyl-2-(4-octylphenyl)-1,3,2-dioxaborolane as a colorless oil. The product was used in the next step without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07902363B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-e2477bd9e1ec49968840cad319376436
출처 메모uspto-grants-2011_03