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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2105605Generated: November 3, 2026

Triethylamine → 2-Bromo-4-(4-tert-butylphenyl)pyridine

https://huagongshe.com/reaction/2105605

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTriphenylphosphineHCID 11776—
ReactantBromineHCID 24408—
ReactantHCID 11424691HCID 11424691—
SolventDichloromethaneHCID 6344—
SolventSodium chloride; waterHCID 57417360—
Product2-Bromo-4-(4-tert-butylphenyl)pyridineHCID 16747829—

Reaction Conditions

Temperature0 °C

Reaction Steps

To triphenylphosphine (Aldrich) (2.4 g, 9.1 mmol) dissolved in 10 mL of CH2Cl2 in a 50-mL round-bottomed flask was added bromine (Aldrich) (0.43 mL, 8.5 mmol). After stirring at 0° C. for 10 min, 4-[4-(tert-butyl)phenyl]pyridine 1-oxide (1.5 g, 6.5 mmol) was added dropwise, followed by Et3N (1.2 mL, 8.5 mmol). The reaction mixture was stirred at 0° C. for 1 h and then at room temperature overnight. Methylene chloride and brine were added, and the aqueous layer was extracted with CH2Cl2. The organic layer was collected and dried over Na2SO4, filtered and concentrated in vacuo. Following purification by silica gel chromatography (10:1 hexane:EtOAc), the title compound was obtained as a pale yellow oil. MS (ESI, pos. ion) m/z: 293 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07579347B2
Source datasetuspto-grants-2009_08
ORD IDord-f8dd12d411a14dd498c9b89b4d2c6a9d
Source noteuspto-grants-2009_08