HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231451Generated: November 3, 2026
Potassium Hydroxide → HCID 20032358, compound
https://huagongshe.com/reaction/231451
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | N-Methoxyacetamide | HCID 138591 | — |
| Reactant | 1-(Bromomethyl)-2-chloro-4-fluorobenzene | HCID 2725062 | — |
| Catalyst | 18-Crown-6 | HCID 28557 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20032358 | HCID 20032358 | 33.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04846882 |
|---|
| Source dataset | uspto-grants-1989_07 |
|---|
| ORD ID | ord-0762b866d1654bfe961474f9b99ac86b |
|---|
| Source note | uspto-grants-1989_07 |
|---|