HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 2-Cyano-4,4,8-trimethyl-non-2-enoic acid benzyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Benzyl 2-cyanoacetate | HCID 560818 | — |
| Reactant | 2,2,6-Trimethyl-heptanal | HCID 21943661 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-Cyano-4,4,8-trimethyl-non-2-enoic acid benzyl ester | HCID 68872461 | 61.6% |
Reaction Steps
To a mixture of 2,2,6-Trimethyl-heptanal (1.05 g, 6.73 mmol), piperidine (0.19 mL, 2.01 mmol) and benzyl cyanoacetate (1.29 g, 7.4 mmol) in toluene (50 mL) was added glacial acetic acid (0.72 g, 12.1 mmol). The flask was fitted with a Dean-Stark trap, and the mixture was heated at reflux for 18. The mixture was cooled, treated with dilute HCl, and the layers were separated. The organics were washed with a saturated sodium bicarbonate solution followed by brine, and dried (MgSO4), filtered and concentrated. The residual oil was purified by silica gel chromatography (98/2 hexane/EtOAc) to give 1.3 g of 2-Cyano-4,4,8-trimethyl-non-2-enoic acid benzyl ester m/z 314 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07419981B2 |
| Source dataset | uspto-grants-2008_09 |
| ORD ID | ord-9dc558629ce14142bf4d4ee6b3962698 |
| Source note | uspto-grants-2008_09 |