戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 30984作成日:2026年10月25日

P-Anisidine → 7-Methoxy-2H-benzo[e][1,2,4]thiadiazin-3(4H)-one 1,1-dioxide

https://huagongshe.com/reaction/30984

反応式

関与物質

役割名称HCID仕込み量
反応物P-AnisidineHCID 7732—
反応物Chlorosulfonyl isocyanateHCID 70918—
反応物Aluminum(III) ChlorideHCID 6451240—
溶媒NitroethaneHCID 6587—
生成物7-Methoxy-2H-benzo[e][1,2,4]thiadiazin-3(4H)-one 1,1-dioxideHCID 1252849095%

反応条件

温度-40 °C

反応手順

A solution of chlorosulfonyl isocyanate (17 mL, 195 mmol.) was dissolved in 150 mL of nitroethane and cooled to −40° C. A solution of 4-methoxyaniline (Z) (20 g, 162 mmol) in 100 mL of nitroethane was then added drop-wise from a dropper funnel with stirring. After the addition was completed, the reaction was stirred for an additional 5 minutes and aluminum chloride (25 g, 195 mmol) was added. The mixture was then quickly heated to 110° C. with stirring for 20 minutes. The crude material was then poured onto ice and the precipitate was collected by suction filtration, washed with cold water, and dried in vacuo to produce 35 g of the desired product (8) as a purple powder in 95% yield. 1H NMR (400 MHz, DMSO-d6): δ 11.05 (s, 1H), 7.2 (m, 3H), 3.78 (s, 3H), 3.6 (br, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07425552B2
出典データセットuspto-grants-2008_09
ORD IDord-6983da0e423f4f0586daf65b5c99150f
出典メモuspto-grants-2008_09