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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448373Generated: October 30, 2026

Potassium Hydroxide → HCID 58307233, compound

https://huagongshe.com/reaction/448373

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant3-(Dimethylamino)-1-propanolHCID 76646—
Reactant5-Fluoro-2-nitroanisoleHCID 2779250—
CatalystTrioctylmethylammonium chlorideHCID 21218—
ProductHCID 58307233HCID 5830723371%

Reaction Conditions

Temperature80 °C

Reaction Steps

3-Dimethylaminopropanol (1.45 g, 14.0 mmol) was added to a mixture of powdered KOH (0.79 g, 14.0 mmol) and Aliquat 336 (0.57 g, 1.4 mmol) and the resulting mixture was stirred for 5 minutes at 80° C. Then 4-fluoro-2-methoxy-1-nitrobenzene (2.0 g, 11.7 mmol) was added, and stirring proceeded at this temperature for 30 minutes. The mixture was cooled and partitioned between methylene chloride (80 mL) and dilute aqueous HCl (80 mL), and the organic layer was extracted with dilute aqueous HCl (2×50 mL). The combined aqueous phases were washed with methylene chloride (3×75 mL), basified (3N NaOH), and extracted with methylene chloride (3×75 mL). The combined organic extracts were washed with water (3×100 mL), dried (MgSO4), and evaporated, providing 2.1 g as a yellow oil, in 71% yield: 1H NMR (CDCl3) δ 1.98 (q, J=6.8 Hz, 6H), 2.25 (s, 6H), 2.45 (t, J=7.0 Hz, 2H), 3.74 (t, J=4.6 Hz, 4H), 3.94 (s, 3H), 4.10 (t, J=6.4 Hz, 2H), 6.48-6.53 (m, 2H), 7.99 (d, J=8.8 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481568B2
Source datasetuspto-grants-2013_07
ORD IDord-4f29c306a603448ebf4c8dca0e25fc99
Source noteuspto-grants-2013_07