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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 412797생성일: 2026년 10월 25일

Butylboronic Acid → 4-Tert-butyl-1-n-butylbenzene

https://huagongshe.com/reaction/412797

반응식

참여 물질

역할이름HCID투입량
반응물Butylboronic AcidHCID 20479—
반응물1-Bromo-4-tert-butylbenzeneHCID 77595—
반응물Potassium FluorideHCID 522689—
촉매(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladiumHCID 6505921—
용매TetrahydrofuranHCID 8028—
생성물4-Tert-butyl-1-n-butylbenzeneHCID 524168115.6%

반응 단계

A 4 ml vial was charged with 4-tert-butylbromobenzene (1.00 mmol), Pd(dba)2 (0.01 mmol, 1 mol %), Ph5FcP(t-Bu)2 (0.02 mmol, 2 mol %), KF (2.02 mmol, powdered) and n-butylboronic acid (1.21 mmol). Anhydrous THF (2 ml) and a stirring bar were added, and the vial was sealed with a cap containing a PTFE septum and removed from the drybox. The reaction mixture was stirred at room temperature for 18 h. After a starting aryl halide was consumed as determined by GC, the reaction solution was cooled to room temperature. Then the reaction solution was adsorbed onto silica gel directly, and the product was isolated by eluting with ethyl acetate/hexanes to give 220 mg (98%) of 4-tert-butyl-1-n-butylbenzene as a colorless oil. Kugelrohl distillation was used for further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06562989B2
출처 데이터셋uspto-grants-2003_05
ORD IDord-b0b34f4f058149808efdfe46009df2f8
출처 메모uspto-grants-2003_05