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HRID 1456630作成日:2026年10月27日

Iodine → 3-iodo-4,5-dihydro-1H-benzo[b]azepin-2(3H)-one

https://huagongshe.com/reaction/1456630

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物HexamethyldisilazaneHCID 13838—
反応物Sodium SulfiteHCID 24437—
反応物1,3,4,5-Tetrahydro-2H-1-benzazepin-2-oneHCID 248580—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物3-iodo-4,5-dihydro-1H-benzo[b]azepin-2(3H)-oneHCID 1103347760.3%

反応条件

温度30 °C

反応手順

A suspension of 34.2 g (212 mmol) of 2,3,4,5tetrahydro-1H-[1]-benzazapin-2-one and 224 mL (171.2 g, 1.06 mol) of hexamethyldisilazane in 400 mL of methylene chloride was heated at reflux for 15 min and cooled to 30° C. Iodine (161.5 g, 636 mmol) was added in one portion, the solution heated at reflux for 2.5 h, cooled, and poured into a 0° C. solution of 88.6 g of sodium sulfite in 800 mL of water, with vigorous stirring. The aqueous phase was separated, extracted with methylene choride and the combined organics were washed with water and concentrated in vacuo to approximately 200 mL. Toluene (800 mL) was added, the solution was concentrated to a slurry, and the product collected on a filter. Drying under vacuum gave 36.7 g (60%) of a tan powder. 1H NMR (300 MHz, CDCl3) d 8.47 (1H, bs), 7.3-7.1 (3H, m), 7.06 (1H, d, J=8 Hz), 4.68 (1H, t, J=8.7 Hz), 2.97 (1H, m), 2.80-2.60 (3H, m).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05843941
出典データセットuspto-grants-1998_12
ORD IDord-d52a91c7557044248d135109a34e5900
出典メモuspto-grants-1998_12