戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1007097作成日:2026年10月26日

Ethyl bromoacetate → 7-Bromo-2H-(1,4)-benzothiazin-3(4h)-one

https://huagongshe.com/reaction/1007097

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl bromoacetateHCID 7748—
反応物Sodium BicarbonateHCID 516892—
反応物2-Amino-5-bromobenzene-1-thiolHCID 1209045—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物7-Bromo-2H-(1,4)-benzothiazin-3(4h)-oneHCID 68906582%

反応手順

A mixture of 2-amino-5-bromo-benzenethiol (20 g, 0.1 mol), ethyl bromoacetate (19 g, 0.1 mol), and sodium bicarbonate (8.8 g, 0.1 mol) in DMF (200 ml) was heated to reflux for 2 hours. The mixture was diluted with water and extracted with ethyl acetate (2×100 mL). The combined organic extracts were washed with water, then brine, dried (MgSO4) and evaporated to obtain the crude 7-bromo-4H-benzo[1,4]thiazin-3-one (20 g, 82%). A small portion of sample was recrystallized from ethanol to afford pure 7-bromo-4H-benzo[1,4]thiazin-3-one: mp 212-213° C.; MS (EI) m/z 243/245 (M+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06794373B2
出典データセットuspto-grants-2004_09
ORD IDord-e50172ae9f6142a88197f249cfba527d
出典メモuspto-grants-2004_09