HuagongsheHuagongshe Chemistry Print Report · For research reference only
Alpha-Methylstyrene → HCID 12551067, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Alpha-Methylstyrene | HCID 7407 | — |
| Reactant | Diethyl bromomalonate | HCID 69637 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Catalyst | Copper bromide (CuBr2) | HCID 24611 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 12551067 | HCID 12551067 | 45.2% |
Reaction Steps
To a solution of α-methylstyrene (570 mL, 4.4 mol), 1,8-diazabicyclo[5.4.0]undec-7-ene (240 mL, 1.6 mol) and copper (II) bromide (9.8 g, 44 mmol) in toluene (700 mL) was added diethyl bromomalonate (210 g, 0.88 mol) at 0° C., and the mixture was stirred for 22 hours at room temperature. The obtained solution was washed with saturated aqueous ammonium chloride solution and saturated aqueous sodium chloride solution, and dried over sodium sulfate. Then, the solution was filtrated and the solvent was evaporated. The obtained residue was separated and purified by silica gel chromatography (hexane:ethyl acetate=20:1) to give the title compound (110 g, yield 45%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07351825B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-77f4c79456294192adc2389d3f0d1b02 |
| Source note | uspto-grants-2008_04 |