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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2270482Generated: October 30, 2026

2-Bromoanisole → HCID 11558102, compound

https://huagongshe.com/reaction/2270482

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromoanisoleHCID 11358—
ReactantTrimethyltin chlorideHCID 14016—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
ProductHCID 11558102HCID 1155810276.6%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a stirring solution of n-BuLi (2.6 mL, 2.5M in hexane, 6.42 mmol) in diethyl ether (2.5 mL) at −78° C. was added 2-bromoanisole (1.0 g, 5.35 mmol) in diethyl ether (2 mL) dropwise. After stirring for 1 h at −78° C., trimethyltin chloride (6mL, 1.0M in THF, 6.42 mmol) was added dropwise. The mixture was allowed to stir an additional 2 h while slowly warming to room temperature. The mixture was then washed with saturated aqueous NaHCO3. The aqueous layer was extracted with diethyl ether (1×5 mL) and the organic layers were combined, dried (MgSO4), filtered and concentrate. The residue was purified by column chromatography (silica gel, hexane) to yield the title compound as a colorless oil (1.11 g, 76%). 1HNMR (400 MHz, CDCl3)δ7.47 (d, 1H), 7.40 (t, 1H), 7.05 (t, 1H), 6.90 (d, 1H), 3.36 (s, 3H), 0.34 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06331542B1
Source datasetuspto-grants-2001_12
ORD IDord-10786cb3f18645b8a60283cedb1bc4d0
Source noteuspto-grants-2001_12