Acetonitrile is a polar aprotic solvent commonly used in SNAr reactions. The choice of solvent can impact the reaction kinetics. Polar aprotic solvents are known to stabilize charged species, and in some cases, they can enhance the reaction rates by stabilizing the transition states.
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3-NITRO-2-(1-PYRROLIDINYL)PYRIDINE
3-(2-oxo-cyclohexanyl)-2-cyclohexene-1-one
N,N-diethyl-4-cyanobenzenesulfonamide
C28H22N8O6
4-(Benzamidoxy)-2-butanone
3,4,4a,8a-Tetrahydro-2H,5H-pyrano[2,3-b]pyran
N-Allyl-N-phenyl-1-amino-2-acetophenone (E/Z)-oxime
C28H36N4O6
2-BROMO-3-CHLORO-1-PROPENE
1-Propanone, 2-hydroxy-1-(4-methoxyphenyl)-
1-(4-Nitro-phenyl)-ethanone oxime
4(2H)-Benzofuranone, 3,5,6,7-tetrahydro-2,6,6-trimethyl-2-phenyl-
(Z)-2-Acetylamino-3-[4-fluoro-1-(toluene-4-sulfonyl)-1H-indol-3-yl]-acrylic acid methyl ester
1-Phospha-1-butyne, 3,3-dimethyl-
4-Iodo-1-methyl-1H-pyrazole
2-(4-chlorobenzoyl)-3-methyl-6-morpholino-3-(tertiary butoxycarbonylmethyl)-2,3-dihydro-1,2,4-triazolo<4,3-b>pyridazine
ethyl 5,8-dibromo-3-phenyl-2-naphthoate
N,N-bis(2-cyano-5-methoxyphenyl)-3-(3-methoxyphenyl)propanamide
Benzene, [(chloroethynyl)thio]-
(4-ETHOXY-PHENYL)-OXO-ACETALDEHYDE
[5-(4-BROMO-PHENYL)-FURAN-2-YL]-METHANOL
C14H12N2S
N-(2-Hydroxy-phenyl)-2-(4-nitro-phenyl)-acetamide
