돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1161887생성일: 2026년 10월 24일

Selenious Acid → 5-Chloro-4-ethoxycarbonylmethyl-2-formyl-indole-1-carboxylic acid methyl ester

https://huagongshe.com/ko/reaction/1161887

반응식

참여 물질

역할이름HCID투입량
반응물Selenious AcidHCID 1091—
반응물5-Chloro-4-ethoxycarbonylmethyl-2-methyl-indole-1-carboxylic acid methyl esterHCID 66820156—
용매Ethyl AcetateHCID 8857—
용매1,4-DioxaneHCID 31275—
생성물5-Chloro-4-ethoxycarbonylmethyl-2-formyl-indole-1-carboxylic acid methyl esterHCID 86603873—

반응 조건

온도100 °C

반응 단계

5-Chloro-4-ethoxycarbonylmethyl-2-methyl-indole-1-carboxylic acid methyl ester (398 mg, 1.28 mmol) is dissolved under an atmosphere of argon in dioxane (18 ml). Selenious acid (331 mg, 2.56 mmol) is added, and the reaction mixture is heated to 100° C. for 18 hours. TLC analysis indicates complete conversion of the starting material. The reaction mixture is diluted with EtOAc and poured on water. The organic layer is washed with saturated aqueous NaCl solution, dried over Na2SO4 and concentrated. The solid residue is purified by FCC (hexane/EtOAc 2:1) to afford the title compound. 1H NMR (DMSO, 400 MHz) δ 1.20 (t, J=6.6 Hz, 3H), 4.09 (s, 3H), 4.12 (q, J=6.6 Hz, 2H), 4.19 (s, 2H), 7.64 (d, J=10.8, 1H), 8.09 (d, J=10.8, 1H), 10.32 (s, 1H); ES-MS: 346.1.1 [M+Na]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07820672B2
출처 데이터셋uspto-grants-2010_10
ORD IDord-8fa564b97d724679a1570eb4d623a91f
출처 메모uspto-grants-2010_10