HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → 2-(1,1-Dimethylethoxy)-N-ethyl-1-naphthalenecarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Reactant | Cyclohexane | HCID 8078 | — |
| Reactant | Magnesium Bromide | HCID 82241 | — |
| Reactant | N-ethyl-1-naphthalenecarboxamide | HCID 4088726 | — |
| Reactant | t-Butylperoxy benzoate | HCID 21744378 | — |
| Reactant | CID 53628100 | HCID 178418400 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(1,1-Dimethylethoxy)-N-ethyl-1-naphthalenecarboxamide | HCID 19602319 | 33% |
Reaction Steps
A solution of 1.3M s-BuLi in cyclohexane (34 mL, 44 mmol) was added dropwise to a -78° C. cooled solution of N-ethyl-1-naphthalenecarboxamide (20 mmol) and TMEDA (6.0 mL, 40 mmol) in THF (100 mL). After 30 min, MgBr2.Et2O (15.5 g, 60 mmol) was added portion wise, and the reaction was briefly warmed to ambient temperature then was recooled to -78° C. After 1 h at -78° C., t-butylperoxy benzoate (4.3 g, 22 mmol) was added. The resulting reaction was warmed to -30° C. and worked up in the usual manner, then was purified by chromatography with 3:7 ethyl acetate/hexanes to afford 1.7 g of desired compound as a white solid, a 33% yield. m.p. 126-127° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05994270 |
| Source dataset | uspto-grants-1999_11 |
| ORD ID | ord-9c54fa92272446849c5eb0d3d0b99cd6 |
| Source note | uspto-grants-1999_11 |