HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → HCID 68913985, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 68919904 | HCID 68919904 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 68913985 | HCID 68913985 | 71.6% |
Reaction Steps
((S)-6-Bromo-1,2,3,4-tetrahydro-naphthalen-2-yl)-carbamic acid tert-butyl ester (4.85 g, 14.87 mmol) was dissolved in dimethylformamide (40 ml). Sodium hydride (50% in oil) (785 mg, 16.35 mmol) was added and stirred for 15 minutes at room temperature. Allyl bromide (1.41 ml, 16.35 mmol) was added and the reaction mixture was stirred at room temperature overnight. To the reaction mixture was added H20 (500 ml) and extracted three times with 100 ml diethylether. The organic layer was dried over magnesium sulfate, filtered, and evaporated to dryness to yield 5.5 g of crude product. The crude product was purified with silica gel chromatography with cyclohexane/ethyl acetate (95:5) as eluent, yielding the purified product (3.9 g, 68%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08969552B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-e891add94999445e9f36b764d066d403 |
| Source note | uspto-grants-2015_03 |