HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromonaphthalene → HCID 14272583, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromonaphthalene | HCID 11372 | — |
| Reactant | Tributyltin Chloride | HCID 15096 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Product | HCID 14272583 | HCID 14272583 | — |
Reaction Steps
2.5 M of n-BuLi (1.9 mL/hexane, 4.83 mmol) was added to 2-bromonaphthalene (1 g, 4.83 mmol/THF (20 mL)) and reacted at −78° C. for 40 minutes under a dry and anaerobic operation condition to form a solution. SnBu3Cl (1.5 mL, 5.31 mmol) was then added to the solution and reacted at −78° C. for 1 hour. After returning to room temperature, the solution was continuously reacted for 8 hours. After the reaction was completed, the solution was extracted by ether (30 mL) and deionized water (50 mL). An organic phase was collected. After removal of ether by a rotary concentrator, the organic phase was purified by reduced-pressure distillation to form a transparent pale yellow oily product (22, 1.68 g, 83%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08759543B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-89f9e07f340b46bdb0c6a65568de6d1c |
| Source note | uspto-grants-2014_06 |