HuagongsheHuagongshe Chemistry Print Report · For research reference only
Propargyl alcohol → 3-Pentadecyl-1-(2-propynyloxy)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Propargyl alcohol | HCID 7859 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Hydrogenated cardanol | HCID 68146 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 3-Pentadecyl-1-(2-propynyloxy)benzene | HCID 15045667 | — |
Reaction Steps
To a solution of 24.4 g (80 mmol) of 3-pentadecylphenol, 4.93 g (88 mmol) of propargyl alcohol and 23.1 g (88 mmol) of triphenylphosphine cooled to 15° C. is added dropwise 15.3 g (13.9 ml, 88 mmol) of diethyl azodicarboxylate. The mixture is stirred for 4.5 hours and then is diluted with water and extracted with hexane (3 times). The hexane extracts are combined, washed with 1N sodium hydroxide and are dried over magnesium sulfate overnight. Filtration and evaporation gives crude oil which is subjected to flash chromatography using hexane as eluting solvent. The appropriate fractions are combined to give the title compound as an oil which solidifies upon standing: mp. 26°-27° C. The product is used without further characterization.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05070207 |
| Source dataset | uspto-grants-1991_12 |
| ORD ID | ord-d6b9cf94a0484c3b9e6002f1a161c67e |
| Source note | uspto-grants-1991_12 |