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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569727Generated: October 29, 2026

Ethanol → 1,4,7-Trioxa-10-azacyclododecane

https://huagongshe.com/reaction/569727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantHCID 766194HCID 766194—
CatalystPalladiumHCID 23938—
SolventHCID 178418361HCID 178418361—
Product1,4,7-Trioxa-10-azacyclododecaneHCID 54581760%

Reaction Steps

A quantity of the 1-benzyl-1-aza-4,7,10-trioxacyclododecane compound (3) prepared in Example 3 (45.1 g, 0.17 mol), ethanol (7 g), and 10% palladium on carbon (0.5 g) were shaken in hydrogen atmosphere at more than 50 psi (1 psi= 6.9×103Pa=0.07 kg cm-2). Hydrogen gas was recharged several times into the reaction chamber to keep the pressure elevated. Shaking was continued until the pressure lowering stopped (4 days). After the palladium carbon was filtered, the solvent was evaporated. The pure compound (4) was sublimed from the residue with gentle heating using a water bath (75°-77° C.; crude material melted at this temperature). The sublimate was white needles and was hygroscopic. Yield 60%; 1HNMR (D2O): δ 2.53-2.70 (t, 4H, N--CH2), 3.5-3.75 (m, 12H, O--CH2), no signal at 7.1 (Ar--H of benzyl group, possible contaminant).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04734376
Source datasetuspto-grants-1988_03
ORD IDord-48e816742bfc436ab7a93fa8d00411a0
Source noteuspto-grants-1988_03