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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161887Generated: October 25, 2026

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

https://huagongshe.com/reaction/1161887

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSelenious AcidHCID 1091—
Reactant5-Chloro-4-ethoxycarbonylmethyl-2-methyl-indole-1-carboxylic acid methyl esterHCID 66820156—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
Product5-Chloro-4-ethoxycarbonylmethyl-2-formyl-indole-1-carboxylic acid methyl esterHCID 86603873—

Reaction Conditions

Temperature100 °C

Reaction Steps

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]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820672B2
Source datasetuspto-grants-2010_10
ORD IDord-8fa564b97d724679a1570eb4d623a91f
Source noteuspto-grants-2010_10