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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 410006Generated: November 1, 2026

2-Bromonaphthalene → HCID 14272583, compound

https://huagongshe.com/reaction/410006

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromonaphthaleneHCID 11372—
ReactantTributyltin ChlorideHCID 15096—
ReactantButyllithiumHCID 178418339—
ProductHCID 14272583HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759543B2
Source datasetuspto-grants-2014_06
ORD IDord-89f9e07f340b46bdb0c6a65568de6d1c
Source noteuspto-grants-2014_06