돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 436006생성일: 2026년 10월 25일

Sodium Hydroxide → 2-Ethyl-3-carboxy-benzo[b]thiophene

https://huagongshe.com/reaction/436006

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물BromineHCID 24408—
반응물2-Ethyl-3-acetyl-benzo[b]thiopheneHCID 21455088—
반응물Sodium BisulfiteHCID 23665763—
용매WaterHCID 962—
용매1,4-DioxaneHCID 31275—
생성물2-Ethyl-3-carboxy-benzo[b]thiopheneHCID 2145508992%

반응 조건

온도0 °C

반응 단계

Into a one-litre flask equipped with a mechanical stirrer and a dropping-funnel were introduced 39 g (0.97 mol) of sodium hydroxide with 270 ml of water. The solution was cooled to 0° C by means of an ice-bath and 20 ml (0.333 mol) of bromine were then added through the dropping-funnel followed by 190 ml of dioxan, care being taken to maintain the temperature at 0° C. Finally, still at the same temperature, a solution of 22.6 g (0.111 mol) of 2-ethyl-3-acetyl-benzo[b]thiophene in 25 ml of dioxan were introduced drop-by-drop. The mixture was then allowed to return to room temperature and stirring was maintained for 2 hours. A solution of sodium bisulphite was then added and the reaction medium was acidified and extracted with ether. The organic phase was washed with water, dried and evaporated to dryness to give 20.2 g of 2-ethyl-3-carboxy-benzo[b]thiophene. Yield 92%; M.P. 136° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04007204
출처 데이터셋uspto-grants-1977_02
ORD IDord-b31d435d497f4e3fbccbea2599042cdf
출처 메모uspto-grants-1977_02