戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1760作成日:2026年10月23日

3-Pyridinecarboxaldehyde → Pyridine, 3-(2,2-dibromoethenyl)-

https://huagongshe.com/ja/reaction/1760

反応式

関与物質

役割名称HCID仕込み量
反応物3-PyridinecarboxaldehydeHCID 10371—
反応物Carbon tetrabromideHCID 11205—
反応物TriphenylphosphineHCID 11776—
溶媒DichloromethaneHCID 6344—
生成物Pyridine, 3-(2,2-dibromoethenyl)-HCID 1133452670%

反応手順

Tetrabromomethane (24.82 g, 0.747 mole) and triphenylphosphine (39.17 g, 0.149 mole) were stirred together in dry methylene chloride (100 mL) for 5 min. at 0° C. under a nitrogen atmosphere. To this mixture was added dropwise pyridine 3-carboxaldehyde (4 g, 0.0373 mole). The solution was then stirred for 45 min. at ambient temperature. The reaction mixture was extracted with aqueous 6N hydrochloric acid (3×25 mL), the aqueous layer basified with solid sodium bicarbonate to pH 8-9 and extracted with chloroform (4×25 mL). The combined organic liquours were dried over anhydrous sodium sulfate, filtered and concentrated on a rotary evaporator to give a dark colored syrup. The crude product was chromatographed on silica gel (70-230 mesh) with chloroform:methanol (95:5) as eluant, to afford a light yellow solid (5.0 g, 70%) which rapidly turned dark on standing.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05726316
出典データセットuspto-grants-1998_03
ORD IDord-b463cdcceaba4202b2513724f75023cf
出典メモuspto-grants-1998_03