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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23411Generated: October 27, 2026

Methyl iodide → 6-methoxy-3-methylsulfanyl-1H-indole

https://huagongshe.com/reaction/23411

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium HydroxideHCID 14797—
Reactant6-methoxy-3-thiocyanato-1H-indoleHCID 22574114—
SolventMethanolHCID 887—
Product6-methoxy-3-methylsulfanyl-1H-indoleHCID 2257407737.9%

Reaction Steps

To a solution of 6-methoxy-3-thiocyanato-1H-indole (0.336 g, 1.64 mmole) and methyl iodide (0.700 g, 4.93 mmole) in methanol (10 ml) was added potassium hydroxide solution (0.164 ml, 10N) at 0° C. The reaction mixture was stirred for 1 h at room temperature. Silica gel (5 g) was added to the reaction mixture and the solvent was removed under reduced pressure. The residue was purified on a column of silica gel, eluting the product with mixtures of ethyl acetate:hexane (1:9 to 1:1). The first product which was eluted was the desired 6-methoxy-3-methylsulfanyl-1H-indole (0.120 g, 37% yield) followed by 6-methoxy-1H-indole-3-thiol (0.126 g). Step 3

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06852726B2
Source datasetuspto-grants-2005_02
ORD IDord-c6e4ec08a77f4c4ebf36a51163d07893
Source noteuspto-grants-2005_02