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ChemicalBook CAS DataBase List N-(1-CYANOCYCLOHEXYL)ACETAMIDE
4550-68-9

N-(1-CYANOCYCLOHEXYL)ACETAMIDE synthesis

3synthesis methods
-

Yield:4550-68-9 52%

Reaction Conditions:

with trimethylamine in diethyl ether at 20;Cooling with ice;

Steps:

1.2 1.2 Synthesis of N-(1 -cyanocyclohexyl)-acetamide

To a stirred solution of aminonitrile (474 mg, 3.62 mmol) and trimethylamine (0.6 mL, 4.28 mmol) in anhydrous Et20 (6 mL) cooled in an ice bath was added dropwise acetyl chloride (0.3 mL, 4.28 mmol) by syringe. The bath was removed and the reaction was stirred at rt for 3.5 hours. Then, the mixture was filtered through a fritted-glass funnel (medium porosity), and the Et20 was discarded. Using a second filter flask, the filter cake was washed 4 times with EtOAc. The EtOAc extracts were collected and evaporated to yield 311.7 mg (52% yield) of target compound as a white solid that did not require purification for subsequent reactions.1H NMR (200 MHz, CDCI3) d 7.08 (s, 1 H), 2.40-2.19 (m, 2H), 1.96 (s, 3H), 1.80-1.40 (m, 8H).

References:

WO2020/94454,2020,A1 Location in patent:Page/Page column 27