返回
化工社化工社化学信息打印报告 · 仅供科研参考
HRID 746292生成日期:2026年10月24日

溴离子(溴化物)标准溶液 → 2-吡啶基硫醚

https://huagongshe.com/zh-CN/reaction/746292

反应方程式

参与物

角色名称HCID投料
反应物溴离子(溴化物)标准溶液HCID 259—
反应物聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯]HCID 962—
反应物氢化钠HCID 24758—
反应物HCID 178418616HCID 178418616—
溶剂N,N-二甲基甲酰胺HCID 6228—
产物2-吡啶基硫醚HCID 521114—

反应步骤

2.22 g of 2-mercaptopyridine and 0.96 g of 50% sodium hydride were dissolved in 50 ml of dimethylformamide, and the mixture was stirred at room temperature for one hour. Thereafter, 13.0 g of polyprenyl bromide of general formula (II) in which n=15 and A=Br were added. After the addition, the mixture was stirred overnight at room temperature. The reaction mixture was poured into about 50 ml of water and extracted with diethyl ether. The diethyl ether layer was washed with water and dried over anhydrous magnesium sulfate. The ether was distilled off to give a yellow liquid. The liquid was purified by silica gel column chromatography using hexane-ethyl acetate as the eluent to give 7.8 g of a slightly yellow liquid. NMR analysis of this liquid demonstrated that the signal (doublet, δ=3.91) assignable to --CH2Br of the starting polyprenyl bromide had disappeared and a signal (doublet, δ=3.78) assignable to --CH2S and a signal (multiplet, δ=6.75-8.35) assignable to --S--C5H4N had newly appeared. FD-MASS of this liquid gave m/e=1335.

来源与证据

DOI10.6084/m9.figshare.5104873.v1
专利号US04603208
来源数据集uspto-grants-1986_07
ORD IDord-6a6f9f37cbd243d89d0cd4c40e4cf230
来源说明uspto-grants-1986_07