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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2389370Generated: October 31, 2026

Trimethylsilyl iodide → HCID 178424150, compound

https://huagongshe.com/reaction/2389370

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl iodideHCID 85247—
ReactantHCID 68538705HCID 68538705—
SolventDichloromethaneHCID 6344—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 178424150HCID 17842415064.7%

Reaction Steps

To a solution of 2-methoxy-5-(2′-methylbiphenyl-2-yl)pyridine (2.20 g) in DCM (50 mL) was added iodo(trimethyl) silane (5.0 g) at ambient temperature. The reaction mixture was stirred at ambient temperature for 4 days. To the reaction mixture was added brine (50 mL). The mixture was extracted with EtOAc and the organic layer was dried over anhydrous MgSO4, filtered and evaporated in vacuo. The residue was purified by silica gel column chromatography (EtOAc:chloroform=3:7) to afford 5-(2′-methylbiphenyl-2-yl)pyridin-2-ol (1.35 g) as pale yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273745B2
Source datasetuspto-grants-2012_09
ORD IDord-1aed091632664b479859c8ab6ad3cc92
Source noteuspto-grants-2012_09