HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-Ethoxyspiro[3.6]decan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ether, ethyl ethynyl | HCID 61239 | — |
| Reactant | Cycloheptanecarbonyl chloride | HCID 12556870 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 3-Ethoxyspiro[3.6]decan-1-one | HCID 21919562 | 87.1% |
Reaction Steps
A solution of cycloheptyl carbonyl chloride (10.0 g, 0.062 mol) and ethoxyacetylene (40% w/w solution in hexanes, 6.0 g, 0.083 mol, 12 ml) in diethylether (50 ml) was treated dropwise with triethylamine (20 ml, 0.14 mol) and the reaction stirred for 5d at room temperature. Filtration and concentration of the filtrate in vacuo followed by chromatography (SiO2, 5:1 EtOAc:hexanes) gave the title compound as a pale yellow oil (10.5 g, 0.054 mol, 87%). δH (CDCl3, 300K) 4.78 (1H, s), 4.20 (2H, q J 7.1 Hz), 1.94-1.87 (2H, m), 1.83-1.77 (2H, m), 1.71-1.66 (2H, m), 1.63-1.52 (6H, m), 1.45 (3H, t J 7.1 Hz); m/z (ES+, 70V) 194.9 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06878718B2 |
| Source dataset | uspto-grants-2005_04 |
| ORD ID | ord-168e60ebf5404699916e1ea3575dd1c6 |
| Source note | uspto-grants-2005_04 |