戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 964565作成日:2026年10月25日

Dibenzofuran → Dibenzofuran, 4-methyl-

https://huagongshe.com/reaction/964565

反応式

関与物質

役割名称HCID仕込み量
反応物DibenzofuranHCID 568—
反応物Dimethyl SulfateHCID 6497—
反応物Ammonium ChlorideHCID 25517—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物Dibenzofuran, 4-methyl-HCID 43489100.2%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05770598
出典データセットuspto-grants-1998_06
ORD IDord-31779468f8784f4498be2fec604b723d
出典メモuspto-grants-1998_06