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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1533859Generated: October 26, 2026

Potassium Hydroxide → 1-(2-Fluoro-6-methoxyphenyl)piperazine

https://huagongshe.com/reaction/1533859

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantSodium HydroxideHCID 14798—
Reactant2-Fluoro-6-methoxyanilineHCID 459253—
ReactantEthanamine, 2-bromo-N-(2-bromoethyl)-, hydrobromide (1:1)HCID 12692731—
SolventWaterHCID 962—
Product1-(2-Fluoro-6-methoxyphenyl)piperazineHCID 1567612177%

Reaction Conditions

Temperature110 °C

Reaction Steps

2-Fluoro-6-methoxyaniline (7.80 g) and 17.23 g of di-(2-bromoethyl)amine hydrobromide were dissolved in 5 ml of water and, by heating at about 110° C. on a bath, 10 ml of 30% potassium hydroxide solution was added thereto (each about 3.5 ml once an hour). Heating was further continued (7 hours in total). After cooled, the reaction solution was made alkaline with aqueous solution of sodium hydroxide to salt out and extracted with chloroform twice. The extract was washed with saturated sodium chloride solution, dried over sodium sulfate, the solvent was evaporated therefrom, and the residue was purified by a column chromatography to give 8.95 g of oily 1-(2-fluoro-6-methoxyphenyl)piperazine in 34.93 g yield or 94%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05086049
Source datasetuspto-grants-1992_02
ORD IDord-4221356c531047a2a9f8568c1e0db29d
Source noteuspto-grants-1992_02