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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231451Generated: November 3, 2026

Potassium Hydroxide → HCID 20032358, compound

https://huagongshe.com/reaction/231451

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantN-MethoxyacetamideHCID 138591—
Reactant1-(Bromomethyl)-2-chloro-4-fluorobenzeneHCID 2725062—
Catalyst18-Crown-6HCID 28557—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 20032358HCID 2003235833.5%

Reaction Steps

To a stirred mixture of 1.95 g (0.0219 mole) of N-methoxyacetamide, 1.23 g 0.022 mole) of powdered potassium hydroxide, and a small amount (~0.05 g) of 18-crown-6 in 10 ml of tetrahydrofuran was added a solution of 5.05 g (0.0226 mole) of 4-fluoro-2-chlorobenzyl bromide in 15 ml of tetrahydrofuran. This mixture was heated at reflux for approximately 17 hours and then was allowed to cool to room temperature. The mixture was diluted with 125 ml of diethyl ether and was washed with an aqueous, saturated sodium chloride solution. The organic phase was dried over anhydrous magnesium sulfate and filtered. The filtrate was evaporated under reduced pressure leaving a yellow oil. This oil was purified by column chromatography on silica gel, eluting with ethyl acetate:n-heptane (25:75) followed by ethyl acetate:n-heptane (50:50) , to yield 1.7 g of N-(2-chloro-4-fluoro-benzyl)-N-methoxyacetamide as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04846882
Source datasetuspto-grants-1989_07
ORD IDord-0762b866d1654bfe961474f9b99ac86b
Source noteuspto-grants-1989_07