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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1732128Generated: November 1, 2026

Methyl iodide → HCID 86741129, compound

https://huagongshe.com/reaction/1732128

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantCarbon DisulfideHCID 6348—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 13653080HCID 13653080—
SolventMethanolHCID 887—
ProductHCID 86741129HCID 8674112925%

Reaction Steps

610 mg of methyl (3S)-8-methyl-1,2,3,4-tetrahydro-β-carboline-3-carboxylate are dissolved in 20 ml of methanol, and 2 ml of a 10% aqueous sodium hydroxide solution are added thereto. The mixture is stirred at room temperature for 3 hours. One ml of a 10% aqueous sodium hydroxide solution and 228 mg of carbon disulfide are added to the mixture, and the mixture is stirred at room temperature for 30 minutes. Then, 355 mg of methyl iodide are adde to the mixture, and the mixture is stirred at the same temperature for 2.5 hours. After the reaction, the mixture is evaporated to remove the solvent. The residue is dissolved in water, and the aqueous solution is extracted with ethyl acetate. The aqueous layer is acidified with 10% HCl, and then extracted with ethyl acetate. The extract is washed with water, dried and then evaporated to remove the solvent. A mixture of ether and n-hexane is added to the residue, and the precipitates are collected. 200 mg of (3S)-8 -methyl-2-(methylthio)thiocarbonyl-1,2,3,4-tetrahydro-β-carboline-3-carboxylic acid are obtained as white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04625032
Source datasetuspto-grants-1986_11
ORD IDord-01af04b662e947acb4c8e7894299a174
Source noteuspto-grants-1986_11