HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylamine → HCID 20314652, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Methyl isobutyrate | HCID 11039 | — |
| Reactant | 2,6-Bis(bromomethyl)naphthalene | HCID 3660010 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 20314652 | HCID 20314652 | — |
Reaction Steps
To a solution of 56 ml of diisopropylamine in 1200 ml of dry tetrahydrofuran at -78° C was added 260 ml of 1.6 M n-butyllithium in hexane. After 1 hr of stirring, 40.4 g of methyl isobutyrate was added dropwise and the solution was stirred another 30 minutes. A 60-g portion of 2,6-bis(bromomethyl)naphthalene was added slowly, and the reaction mixture was stirred overnight and then brought to room temperature. Tetrahydrofuran was removed by evaporation. The residue was dissolved in 300 ml of CHCl3, washed 3 times with 400 ml of H2O, and dried and evaporated to dryness to obtain 56 g of 2,6-bis(2-carbomethoxy-2-methylpropyl)naphthalene, m.p. 108°-110° C. The product was recrystallized from benzene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04065431 |
| Source dataset | uspto-grants-1977_12 |
| ORD ID | ord-a80ff6214323423795b3d8d06eda1b26 |
| Source note | uspto-grants-1977_12 |