HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1492086Generated: October 25, 2026
Hexamethylenetetramine → 4-Nonylbenzaldehyde
https://huagongshe.com/reaction/1492086
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexamethylenetetramine | HCID 4101 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | n-Nonylbenzene | HCID 14126 | — |
| Product | 4-Nonylbenzaldehyde | HCID 10933364 | 57% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05371284 |
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| Source dataset | uspto-grants-1994_12 |
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| ORD ID | ord-859f6f1e6fac4fc288830c849b4579ba |
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| Source note | uspto-grants-1994_12 |
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