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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1874880Generated: November 1, 2026

Trimethylsilyldiazomethane → methyl 6-hydroxy-1H-indole-2-carboxylate

https://huagongshe.com/reaction/1874880

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyldiazomethaneHCID 167693—
Reactant6-Hydroxy-1H-indole-2-carboxylic acidHCID 22350191—
SolventMethanolHCID 887—
Productmethyl 6-hydroxy-1H-indole-2-carboxylateHCID 1053570986%

Reaction Steps

A 2M solution of trimethylsilyldiazomethane in hexanes was added to a solution of 6-hydroxy-1H-indole-2-carboxylic acid (0.500 g, 2.82 mmol) in MeOH until the solution remained yellow in color. The solution was stirred at RT until the starting material was consumed as evident by TLC. The reaction mixture was partitioned between water and EtOAc then the organic layer was separated, dried over MgSO4, filtered and concentrated. Purification was accomplished by column chromatography (EtOAc/hexanes) to afford the title compound (0.464 g, 86% yield). 1H NMR (400 MHz, Acetone-d6): δ ppm 10.55 (br. s., 1H), 8.32 (s, 1H), 7.50 (d, 1H), 7.09 (d, 1H), 6.95 (d, 1H), 6.74 (dd, 1H), 3.85 (s, 3H). MS m/z=191.9 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304419B2
Source datasetuspto-grants-2012_11
ORD IDord-8b4e91699266435dabd449cde3668a6f
Source noteuspto-grants-2012_11