HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium diisopropylamide → HCID 68534124, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | HCID 10921941 | HCID 10921941 | — |
| Reactant | 2-Iodobenzyl Bromide | HCID 11426472 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68534124 | HCID 68534124 | — |
Reaction Steps
At −78° C., lithium diisopropylamide solution (2 M in THF/n-heptane, 17 ml, 34 mmol) was slowly added dropwise to ethyl(tert-butoxycarbonylmethylamino)acetate (7.4 g, 34 mmol) in tetrahydrofuran (abs., 50 ml). The mixture was stirred at this temperature for 2 h. 1-Bromomethyl-2-iodobenzene (10.0 g, 46 mmol) was then slowly added dropwise, and the mixture was stirred at −78° C. for 1 h. The reaction solution was slowly (12 h) warmed to room temperature and then concentrated on a rotary evaporator. The residue was taken up in ethyl acetate, washed, dried and concentrated. The residue obtained in this manner was then purified by column chromatography (SiO2, hexane/ethyl acetate). This gave 6.4 g (43%) of the target compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08450301B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-07ec0adea2f046268bac032586af9dd5 |
| Source note | uspto-grants-2013_05 |