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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1870554Generated: October 29, 2026

3-Phenoxyphenol → HCID 18696603, compound

https://huagongshe.com/reaction/1870554

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-PhenoxyphenolHCID 12842—
Reactant2-Chloro-3-nitropyridineHCID 79613—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18696603HCID 18696603—

Reaction Steps

3-Phenoxyphenol (3 g, 16.1 mmol) was added to a solution of potassium t-butoxide (1.90 g of 90%, 16.6 mmol) in 50 mL of dry tetrahydrofuran at room temperature after which the reaction was stirred at room temperature for 10 min. Then, 2-chloro-3-nitropyridine (2.56 g, 16.1 mmol) was added. The reaction mixture was stirred at room temperature for 16 h. The reaction mixture was concentrated under reduced pressure. The residue was diluted with water, extracted twice with methylene chloride and dried over magnesium sulfate. The solvent was then removed to yield the title compound of Step A as an oil. 1H NMR (CDCl3 ; 300 MHz): δ 6.85 (m,1H), 6.90 (m,2H), 7.0-7.2 (m,4H), 7.3-7.4 (m,3H), 8.35 (m,2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06096895
Source datasetuspto-grants-2000_08
ORD IDord-780f50016f414e4d816d4b636f3f798d
Source noteuspto-grants-2000_08