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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1682140Generated: October 30, 2026

Methyl iodide → HCID 14801186, compound

https://huagongshe.com/reaction/1682140

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium sulfide nonahydrateHCID 73972—
ReactantHCID 14801185HCID 14801185—
SolventEthanolHCID 702—
ProductHCID 14801186HCID 1480118692.7%

Reaction Steps

29.1 g (0.14 mol) of 3-methoxymethyl-2-methyl-4-thiocyanoaniline was dissolved in 200 ml of ethanol and mixed with 100 ml of an aqueous solution containing 33.6 g of sodium sulfide nonahydrate at room temperature. Then, 21.9 g of methyl iodide was dropwise added thereto, and the mixture was reacted at room temperature for 3 hours. After completion of the reaction, the solvent was distilled off under reduced pressure, and water and chloroform were added to the residue. Then, the organic layer was separated and washed sequentially with water and a saturated sodium chloride aqueous solution and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure to obtain 25.6 g of the desired product as an oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05175299
Source datasetuspto-grants-1992_12
ORD IDord-c1a6204a7bb544889054d8069b5462f6
Source noteuspto-grants-1992_12