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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161884Generated: October 25, 2026

Acetic Acid → 4-Amino-5-chloro-2-methyl-indole-1-carboxylic acid methyl ester

https://huagongshe.com/reaction/1161884

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSulfuric AcidHCID 1118—
Reactant5-Chloro-2-methyl-4-nitro-indole-1-carboxylic acid methyl esterHCID 66820264—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
Product4-Amino-5-chloro-2-methyl-indole-1-carboxylic acid methyl esterHCID 66819957—

Reaction Conditions

Temperature85 °C

Reaction Steps

5-Chloro-2-methyl-4-nitro-indole-1-carboxylic acid methyl ester (2.1 g, 7.81 mmol) is dissolved in ethanol (40 ml) and glacial acetic acid (40 ml). Iron powder (1.74 g, 31.26 mmol, activated previously with H2SO4 conc and then washed with water) is added, and the reaction mixture is heated to 85° C. for 90 minutes. The reaction mixture is poured into water and stirred at RT for 30 minutes, after which a slightly brownish colored precipitate forms which is filtered off. After washing with water and drying, the title compound is obtained in pure form. 1H NMR (DMSO, 400 MHz, 120° C.) δ 2.51 (s, 3H), 4.05 (s, 3H), 5.0-5.2 (br s, 2H), 6.66 (s, 1H), 7.05 (d, J=9 Hz, 1H), 7.31 (d, J=9 Hz, 1H); ES-MS: 238 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820672B2
Source datasetuspto-grants-2010_10
ORD IDord-d5a07c42aa6c43d09299c5f96a3180f3
Source noteuspto-grants-2010_10