HuagongsheHuagongshe Chemistry Print Report · For research reference only
Homoallyl bromide → HCID 89872739, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Homoallyl bromide | HCID 21241 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl 2-(4-bromophenyl)acetate | HCID 316783 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 89872739 | HCID 89872739 | 89% |
Reaction Steps
To a solution of methyl 4-bromophenylacetate (1 g, 4.37 mmol) in DMF (12 ml) at room temperature was added 60% NaH (0.227 g, 5.68 mmol) and the mixture was stirred at room temperature for 1 hr then was added 4-bromo-1-butene (0.487 ml, 4.80 mmol). The reaction was stirred at room temperature overnight. The reaction was quenched by sat. aq. NH4Cl and was extracted with EtOAc. The combined organic layer was washed with brine and dried over anhydrous sodium sulfate, filtered and concentrated. The residue was purified by flash chromatography (0 to 30% DCM/Hep) to give the title compound 1.1 g (yield 89%). Retention time 1.54 min (condition A).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09108956B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-99ca6cba9ba14c65864776e7f69e571e |
| Source note | uspto-grants-2015_08 |