戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 466822作成日:2026年10月26日

Iodine → 5-(2-Iodophenyl)-2-triphenylmethyltetrazole

https://huagongshe.com/reaction/466822

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物HexaneHCID 8058—
反応物5-Phenyl-2-trityltetrazoleHCID 3292959—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物5-(2-Iodophenyl)-2-triphenylmethyltetrazoleHCID 1895435844.9%

反応条件

温度-10 °C

反応手順

To a solution of 0.5 g (1.3 mmoles) of 18a in 10 mL dry THF cooled to -20° C. under a nitrogen atmosphere was added dropwise with stirring 0.55 mL of 2.5M n-butyl lithium in hexane (1.4 mmoles). When addition was complete, the reaction was allowed to warm to -10° C. over one hour, held there one hour, then cooled to -78° C. After stirring a few minutes, 0.4 g (1.57 mmole) of I2 was added all at once, and stirring continued. After 1 hour the reaction mixture was allowed to warm to ambient temperature. After removal of the solvent, the residue was partitioned between CHCl3 and 1M KH2PO4. The aqueous phase was extracted two more times, the combined organic phases washed with sufficient aqueous Na2S2O3 to remove excess I2, dried (MgSO4) and the solvent evaporated. The residue was crystallized from CH2Cl2 /ether to give 0.3 g product,

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05157040
出典データセットuspto-grants-1992_10
ORD IDord-8c63c4fd92044c4b84daf7e2e491b3be
出典メモuspto-grants-1992_10