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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 4312Generated: October 25, 2026

Iodine → 5-Methoxy-3-cyanomethylthioindole

https://huagongshe.com/reaction/4312

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantChloroacetonitrileHCID 7856—
Reactant5-MethoxyindoleHCID 13872—
ReactantThioureaHCID 2723790—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product5-Methoxy-3-cyanomethylthioindoleHCID 1409695042%

Reaction Steps

To a solution of 50 g (0.34 mole) of 5-methoxyindole and 25.8 (0.34 mole) of thiourea in 1700 ml of 50% aqueous methanol was added 340 ml of KI/I2 in water over a 5 minute period and the reaction mixture was allowed to stir at room temperature for 3 hours. The reaction mixture was then evaporated in vacuo to about 1100 ml, 68 ml of 50% aqueous NaOH were added under nitrogen, the temperature brought to 85° and the mixture was stirred at 80°-90° for 40 minutes. The mixture was cooled and filtered through glass wool and under nitrogen, 21.2 ml (25.4 g; 0.34 mole) of chloroacetonitrile were added. The reaction was allowed to proceed under N2 for 18 hours after which the reaction mixture was layered over with about 800 ml of diethyl ether and the ether was separated off having dissolved a large portion of suspended solid material. The aqueous solution was extracted three times with 500 ml portions of ether which were combined with the other washings and dried over anhydrous K2CO3. The ether layer was filtered and evaporated in vacuo to 33 g of 5-methoxy-3-cyanomethylthioindole (42% yield) as a tan solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04725604
Source datasetuspto-grants-1988_02
ORD IDord-adafda2f10aa459986df317fa2d32be6
Source noteuspto-grants-1988_02