HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1461575Generated: November 1, 2026
Toluene → 4,7,9,9-Tetramethyldec-3-enenitrile
https://huagongshe.com/reaction/1461575
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Cyanoacetic acid | HCID 9740 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | 2,5,7,7-Tetramethyloctanal | HCID 19981043 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4,7,9,9-Tetramethyldec-3-enenitrile | HCID 53805129 | 91.2% |
Reaction Steps
438 g (2.38 moles) of 2,5,7,7-tetramethyloctanal, 202 g (2.38 moles) of cyanoacetic acid, 350 ml of toluene, 350 ml of dimethylformamide and 28.5 g of ammonium acetate were heated under a water separator for 4 h, while stirring. Thereafter, the toluene was distilled off and the remaining residue was heated for 2 h at 180° C. The cooled residue was poured onto ice water and 10 extracted with diethyl ether. The organic phase was washed in succession with NaHCO: solution and water and then distilled. 450 g (yield: 91% of theory) of 4,7,9,9-tetramethyldec-3-enenitrile of boiling point 83°-88° C./-.3 mbar were obtained. The fragrance note was waxy, floral and fresh.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05075489 |
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| Source dataset | uspto-grants-1991_12 |
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| ORD ID | ord-b04c9731b4074a9fbf1f665ed9302cec |
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| Source note | uspto-grants-1991_12 |
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