Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane | HCID 5017741 | — |
| 반응물 | 1-Iodo-4-octylbenzene | HCID 11594836 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 4,4,5,5-Tetramethyl-2-(4-octylphenyl)-1,3,2-dioxaborolane | HCID 58823386 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US07902363B2 |
|---|
| 출처 데이터셋 | uspto-grants-2011_03 |
|---|
| ORD ID | ord-e2477bd9e1ec49968840cad319376436 |
|---|
| 출처 메모 | uspto-grants-2011_03 |
|---|