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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1492086Generated: October 25, 2026

Hexamethylenetetramine → 4-Nonylbenzaldehyde

https://huagongshe.com/reaction/1492086

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexamethylenetetramineHCID 4101—
ReactantTrifluoroacetic acidHCID 6422—
Reactantn-NonylbenzeneHCID 14126—
Product4-NonylbenzaldehydeHCID 1093336457%

Reaction Conditions

Temperature25 °C

Reaction Steps

Oxidative Formylation--Allow a two-phase mixture of trifluoroacetic acid (150 mL) and hexamethylene tetramine (14.0 g, 0.100 mol), and 1-phenyl-n-nonane (20.4 g, 0.100 mol) to stand 18 hrs. at 25° C., and then reflux for 22 hrs. Concentrate the homogenous reaction mixture and pour the residue over ice and H2O (total of 600 mL). Add diethyl ether (200 mL) and stir the mixture vigorously for 30 min. Raise the pH of the mixture to pH 8 with solid Na2CO3, and add diethyl ether (200 mL). Shake the layers and separate. Extract the aqueous phase with diethyl ether. Wash the combined organic solutions with H2O and brine, dry and filter. Evaporate the solvent, and distill the residue to give 4-(n-nonyl)benzaldehyde (57% yield, 13.2 g) b.p. 136°-139° C. at 0.55 mm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05371284
Source datasetuspto-grants-1994_12
ORD IDord-859f6f1e6fac4fc288830c849b4579ba
Source noteuspto-grants-1994_12