戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 36791作成日:2026年10月26日

Sodium Iodide → 1-(Phenyloxycarbonyloxy)pentyl 5-(N-acetylamino)-3-(N-acetyl-N-methylamino)-2,4,6-triiodobenzenecarboxylate

https://huagongshe.com/reaction/36791

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium IodideHCID 5238—
反応物1-Chloropentyl phenyl carbonateHCID 19422763—
反応物potassium 5-(N-acetylamino)3-(N-acetyl-N-methylamino)-2,4,6-triiodobenzenecarboxylateHCID 23717801—
溶媒DimethylformamideHCID 6228—
生成物1-(Phenyloxycarbonyloxy)pentyl 5-(N-acetylamino)-3-(N-acetyl-N-methylamino)-2,4,6-triiodobenzenecarboxylateHCID 19422761—

反応条件

温度50 °C

反応手順

1-Chloropentyl phenyl carbonate (0.14 g, 0.58 mmol) was added at room temperature to a solution of potassium 5-(N-acetylamino)-3-(N-acetyl-N-methylamino)-2,4,6-triiodobenzenecarboxylate (0.35 g, 0.53 mmol) and sodium iodide (0,008 g, 0.053 mmol) in dry DMF (3 ml). After stirring at 50° C. for 5 hours and at room temperature for 2 days the solvent was removed at reduced pressure. The residue was suspended in chloroform (15 ml) and washed four times with a saturated sodium hydrogen carbonate solution and finally twice with water. After drying with magnesium sulfate the solution was evaporated to dryness. Yield: 0.04 g. Purity by HPLC: 94.8% 1H-NMR (DMSO-d6): delta=0.92(CH3CH2); 1.31-1.55 (CH3CH2CH2); 1.68 (NCH3COCH3); 2.04 (CH2CH); 2.05 (NHCOCH3); 2.97 (NCH3); 6.95 (CH); 7.27-7.49 (phenyl); 10.13 ppm (NH). FAB/MS: 835 ((M+H)+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05416223
出典データセットuspto-grants-1995_05
ORD IDord-c317ffa6ffad4aabb1fe837f8f4d02de
出典メモuspto-grants-1995_05