Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Nitromethane | HCID 6375 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 86596725 | HCID 86596725 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86596724 | HCID 86596724 | — |
Reaction Steps
0.485 mol (75.8 g) of the (2E)-5-methyl-hex-2-ene carboxylic acid ethyl ester produced according to 2.1. were dissolved under a nitrogen atmosphere in THF (abs.). 0.73 mol (39.1 ml) of nitromethane and 0.49 mol (485 ml) of a 1 molar tetrabutylammonium fluoride solution in THF were added, wherein an orange solution arose. The mixture was refluxed for 20 hours. After cooling, the mixture was combined with 280 ml of water and extracted four times with diethyl ether. The organic phase was extracted three times with 10% aqueous potassium hydrogensulfate solution and washed to neutrality with water. The organic phase was dried with magnesium sulfate and evaporated in a rotary evaporator. An orange liquid was obtained. The crude yield amounted to 95.2 g (90% of theoretical).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07141695B2 |
|---|
| Source dataset | uspto-grants-2006_11 |
|---|
| ORD ID | ord-caa93c1016824689ba03f386eb1afe8f |
|---|
| Source note | uspto-grants-2006_11 |
|---|