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ChemicalBook CAS DataBase List 4-CYANO-2-METHOXYPYRIDINE
72716-86-0

4-CYANO-2-METHOXYPYRIDINE synthesis

5synthesis methods
2-Chloro-4-cyanopyridine

33252-30-1

Sodium Methoxide

124-41-4

4-CYANO-2-METHOXYPYRIDINE

72716-86-0

General procedure for the synthesis of 4-cyano-2-methoxypyridine from 2-chloro-4-cyanopyridine and sodium methanol: To a solution of 2-chloro-4-cyanopyridine (1.38 g, 10 mmol) in dioxane (10 mL) was added a methanolic solution of sodium methanol (25%, 2.27 g, 10.5 mmol). The reaction mixture was heated to reflux for 5 h, followed by cooling to room temperature and standing overnight in a refrigerator. The precipitate was collected by filtration and washed with methanol. The filtrate was concentrated to about 10 mL and water (100 mL) was added. The precipitate was collected by filtration again and washed with water to give 4-cyano-2-methoxypyridine (1.93 g, 72% yield) as a white solid. Mass spectrum (electrospray positive ion mode) m/z 135 [M + H]+.

33252-30-1 Synthesis
2-Chloro-4-cyanopyridine

33252-30-1
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Yield: 51%

Reaction Conditions:

with sodium in methanol;methanoldioxan;water

Steps:

3.a EXAMPLE 3
(a) Sodium (20.8 g) was dissolved in methanol (285 ml), a solution of 2-chloro-4-cyanopyridine (115.53 g) in methanoldioxan (1:1, 850 ml) was added and the mixture was boiled under reflux for 21/2 hours and was allowed to cool. The mixture was filtered and the volume of the filtrate was reduced by evaporation in 200 ml and water (400 ml) was added. The solid which precipitated out was filtered off to give 2-methoxy-4-cyanopyridine (57.2 g, 51%), m.p. 93-95.5°.

References:

Smith Kline & French Laboratories Limited US4255428, 1981, A

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