戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 477281作成日:2026年10月24日

Bromide ion → 2,2'-Thiodipyridine

https://huagongshe.com/ja/reaction/477281

反応式

関与物質

役割名称HCID仕込み量
反応物Bromide ionHCID 259—
反応物WaterHCID 962—
反応物Sodium hydrideHCID 24758—
反応物HCID 178418616HCID 178418616—
溶媒DimethylformamideHCID 6228—
生成物2,2'-ThiodipyridineHCID 521114—

反応手順

1.11 g of 2-mercaptopyridine and 0.48 of 50% sodium hydride were dissolved in 25 ml of dimethyl formamide, and the mixture was stirred at room temperature for 1 hour. A solution of 6.5 g of polyprenyl bromide of general formula (II) in which n is 15 and A2 is Br in 5 ml of N,N-dimethylformamide was added dropwise. 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. Then, 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 an eluent to give 3.9 g of a slightly yellow liquid. The NMR analysis of this liquid showed that the signal (doublet, δ=3.91) assigned to --CH2Br of the starting polyprenyl bromide disappeared, and a signal (doublet, δ=3.78) assigned to --CH2S and a signal (multiplet, δ=6.75-8.35) assigned to --S--C5H4N newly appeared. The FD-MASS analysis of this liquid gave m/e=1335.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04886904
出典データセットuspto-grants-1989_12
ORD IDord-640a5ddae68c430d83240f7492a69123
出典メモuspto-grants-1989_12