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874482-94-7

Benzonitrile, 2-chloro-4-(trifluoromethoxy)- synthesis

5synthesis methods
Methanesulfonic acid, 1,1,1-trifluoro-, 2-chloro-4-(trifluoromethoxy)phenyl ester

653578-64-4
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Benzonitrile, 2-chloro-4-(trifluoromethoxy)-

874482-94-7
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Yield:874482-94-7 220 mg

Reaction Conditions:

with tetrakis(triphenylphosphine) palladium(0) in N,N-dimethyl-formamide at 120; for 2 h;Inert atmosphere;

Steps:

B SteQ B. 2-Choro-4-(trfluoromethoxy)benzonftre.

2-Choro-4-(trfl uoromethoxy) phenytrfluoromethanesufonate was dssoved n DM F (4.0 mL), foflowed by add Won of zinc cyanide (681 mg, 5.8 mmo) and (Pd(PPh3)4) (335 mg, 0.3 mmo). The reacfionmixture was degassed w[th nftrogen for 10 rnnutes and then heated at 120 C for 2h. After coohng to rt, the crude reacUon mixture was duted w[th saturated aqueous NaHCO3 souUon, and extracted w[th EtOAc (x 3). The combined organic extracts were dried over Na2SO4 and concentrated. PurWcaUon (FCC, SO2 0-5% EtOAc/hexanes) provided the tWe compound as an oH (220 mg, 34% yed). 1H NMR (500 MHz, DMSO-d6) ? 8.16 (d, J =8.7 Hz, I H), 7.93 (dd, J = 2.2, 1.0 Hz, I H), 7.66 -6.56 (m, 1 H),

References:

WO2016/176463,2016,A1 Location in patent:Page/Page column 67

773837-37-9 Synthesis
sodium:cyanide

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69695-61-0 Synthesis
2-CHLORO-4-(TRIFLUOROMETHOXY)ANILINE

69695-61-0
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Benzonitrile, 2-chloro-4-(trifluoromethoxy)-

874482-94-7
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