HuagongsheHuagongshe Chemistry Print Report · For research reference only
Homoallyl bromide → HCID 12045755, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Homoallyl bromide | HCID 21241 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-Methoxyindan-1-one | HCID 78787 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 12045755 | HCID 12045755 | — |
Reaction Steps
To a solution of 5-methoxy-1-indanone (1 g, 6.17 mmol) in DMF (6 mL) at rt was added NaH (740 mg, 61% in oil, 18.5 mmol) and 4-bromo-1-butene (2.5 mL, 24.7 mmol). After 20 h at rt, the solution was diluted with CH2Cl2 and quenched with saturated aqueous NH4Cl. The slurry was dried with MgSO4 and filtered through a plug of silica and rinsed with 10% EtOAc in hexanes. The filtrate was concentrated and provided crude 2,2-di(3-butenyl)-5-methoxy-1-indanone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06800785B1 |
| Source dataset | uspto-grants-2004_10 |
| ORD ID | ord-082eab2f9fbe43bdb30ea1095ed79018 |
| Source note | uspto-grants-2004_10 |