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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1650688Generated: November 1, 2026

Methyl iodide → HCID 19612501, compound

https://huagongshe.com/reaction/1650688

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 178420778HCID 178420778—
SolventEthanolHCID 702—
ProductHCID 19612501HCID 1961250130%

Reaction Steps

5-(3-pyridyl)-tetrazole (11) (J. M. McManus and R. M. Herbst, J. Am. Chem. Soc., 24 (1959) 1462-64) (10 g, 0.068 mol), sodium hydroxide (2.73 g, 0.068 mol), and methyl iodide (14.5 g, 0.1 mol) in ethanol (100 ml) was stirred at 40° C. overnight. The mixture was filtered and the filtrate was evaporated. The residue was dissolved in dichloromethane (100 ml), and the solution was washed three times with water (100 ml). The organic phase was dried over magnesium sulphate and evaporated yielding 3.21 g (0.020 mol, 30%) of 12 with M.P. 108°-110° C. According to the 1H NMR spectrum the product contained less than 10% of the 1-isomer.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04925858
Source datasetuspto-grants-1990_05
ORD IDord-926e8615535d41789ba9db47e85cf254
Source noteuspto-grants-1990_05