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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 964565생성일: 2026년 10월 24일

Dibenzofuran → Dibenzofuran, 4-methyl-

https://huagongshe.com/ko/reaction/964565

반응식

참여 물질

역할이름HCID투입량
반응물DibenzofuranHCID 568—
반응물Dimethyl SulfateHCID 6497—
반응물Ammonium ChlorideHCID 25517—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물Dibenzofuran, 4-methyl-HCID 43489100.2%

반응 단계

Dibenzofuran (26.94 g, 160 mmol) was dissolved in dry THF (500 ml) and cooled to -78° C. n-Butyl lithium (1.6M in hexane, 200 ml, 320 mmol) was added in portions over 30 mins. and the solution was allowed to warm to room temperature over 2.5 hours. The solution was recooled to -70° C. and a mixture of dimethyl sulphate (32 ml, 340 mmol) in dry THF (100 ml) was added dropwise. Once the addition was complete, the reaction was allowed to warm to room temperature, stirred for 18 hours and poured onto saturated ammonium chloride solution (400 ml). The phases were separated and the aqueous extracted twice with ether. The combined organic phases were dried (MgSO4) and evaporated in vacuo. Chromatography on silica (eluting with 40-60 petrol) gave the pure product as a clear oil (29.2 g, 100%) δH [2H6 ]-DMSO 8.1 (1H, d), 7.9 (1H, d), 7.7 (1H, d),7.5 (1H, t), 7.4 (1H, t), 7.25 (2H, m), 2.55 (3H, s).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05770598
출처 데이터셋uspto-grants-1998_06
ORD IDord-31779468f8784f4498be2fec604b723d
출처 메모uspto-grants-1998_06