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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 547842Generated: October 25, 2026

Cyclohexylamine → 2-((1-Aminocyclohexyl)methylamino)-2-(hydroxymethyl)propane-1,3-diol

https://huagongshe.com/reaction/547842

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexylamineHCID 7965—
ReactantEthyl AcetateHCID 8857—
Reactant(1-Aminocyclohexyl)methanolHCID 409153—
Reactant1,3-OxazolidineHCID 536683—
Product2-((1-Aminocyclohexyl)methylamino)-2-(hydroxymethyl)propane-1,3-diolHCID 67163584—

Reaction Steps

The reactor mixture is filtered to remove the catalyst; the filtrate is clear and pale yellow. The methanol and water are removed from the filtrate by rotary evaporation to give 80.6 grams of an off-white paste product. GC analysis shows this product to contain nearly 20% of residual TA. This product is mixed with 500 mL of ethyl acetate, and the mixture is heated to reflux for about 15 minutes. The mixture is cooled to room temperature, then it is filtered free of the TA solids. The solids are washed on the filter with ethyl acetate, then the combined filtrate and washings are solvent stripped by rotary evaporation to give 67.7 grams (76%) of TA-ACyHM as a very viscous oil. GC analysis shows a product purity of >98%, with traces of cyclohexylamine, 1-aminocyclohexanemethanol (ACyHM), and oxazolidine byproduct. GC/MS, IR, 1H- and 13C-NMR analyses are consistent with the desired structure. Titration gives pK1=9.7 and pK2=4.5. Volatility by the modified EPA Test Method 24 is 3.8%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07939589B2
Source datasetuspto-grants-2011_05
ORD IDord-15f10658c30c4bddb356e500522037f0
Source noteuspto-grants-2011_05