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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1588046Generated: October 31, 2026

Diazomethane → Diazomethane

https://huagongshe.com/reaction/1588046

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiazomethaneHCID 9550—
ReactantPotassium HydroxideHCID 14797—
ReactantCyclohexanecarbonyl chlorideHCID 75938—
ReactantN-Methyl-N'-nitro-N-nitrosoguanidineHCID 135436526—
SolventDiethyl EtherHCID 3283—
ProductDiazomethaneHCID 9550—
ProductHCID 53903884HCID 53903884—

Reaction Steps

A solution of diazomethane is prepared from N-methyl-N'-nitro-N-nitroso guanidine (12.5 g), potassium hydroxide (50%, 20 ml), and ether (300 ml). TEA (7.7 ml) is added to the diazomethane solution (65%) followed by cyclohexane carboxylic acid chloride (7.4 ml) slowly at 0° . The reaction is stirred at 0° for 1 hr then for 18 hrs at 22° . A porecipitate forms, it is filtered and washed with ether, and the filtrate concentrated. The resulting oil is cooled to -78° , triturated with ether, then warmed to 22° and concentrated with reduced pressure and heat to give the title compound as an oil, NMR (acetone-d6) 5.4 and 1.4-0.8 δ.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05220021
Source datasetuspto-grants-1993_06
ORD IDord-511508def6a047a6bd8e2f60f8f13887
Source noteuspto-grants-1993_06