HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → Methyl 2-ethyl-2-(1-methylethyl)-4-pentenoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Hexamethylphosphoramide | HCID 12679 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | Methyl 2-ethyl-3-methylbutyrate | HCID 12696465 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 2-ethyl-2-(1-methylethyl)-4-pentenoate | HCID 10607559 | 82% |
Reaction Steps
The reaction of methyl 2-ethyl-3-methylbutyrate (23.76 g, 165 mmol), prepared as in Lion C, Dubois J E (1981) supra., with allyl bromide (31.34 g, 259 mmol) in the presence of lithium diisopropylamide (prepared by treating diisopropylamine (25.05 g, 248 mmol) with butyllithium in hexanes (2.5 M, 94.4 mL, 236 mmol)) in THF (330 mL) and HMPA (24.7 mL, 142 mmol), as described above in the preparation of Example 7, followed by the vacuum distillation of crude product afforded the pure olefinic ester (24.85 g, 82%) as a colorless liquid: bp 92-94° C. (20 mmHg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06066666 |
| Source dataset | uspto-grants-2000_05 |
| ORD ID | ord-2eacac5ad4454b9ba4977bd957c5d517 |
| Source note | uspto-grants-2000_05 |