4-(Morpholinomethyl)benzonitrile

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4-(Morpholinomethyl)benzonitrile Basic information
Product Name:4-(Morpholinomethyl)benzonitrile
Synonyms:4-MORPHOLIN-4-YLMETHYLBENZONITRILE;4-(4-MORPHOLINYLMETHYL)BENZONITRILE;p-Tolunitrile, alpha-(4-morpholinyl)-;4-MORPHOLIN-4-YLMETHYLBENZONITRILE, 95+%;USAF A-3730;4-(4-Morpholinylmethyl)benzonitrile,97%;4-(morpholin-4-ylmethyl)benzonitrile hydrochloride;benzonitrile, 4-(4-morpholinylmethyl)-
CAS:37812-51-4
MF:C12H14N2O
MW:202.25
EINECS:
Product Categories:Aromatic Nitriles
Mol File:37812-51-4.mol
4-(Morpholinomethyl)benzonitrile Structure
4-(Morpholinomethyl)benzonitrile Chemical Properties
Melting point 84-89°C
Boiling point 332.4±32.0 °C(Predicted)
density 1.14±0.1 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka5.94±0.10(Predicted)
form Crystalline Powder
color White to light yellow
InChI1S/C12H14N2O/c13-9-11-1-3-12(4-2-11)10-14-5-7-15-8-6-14/h1-4H,5-8,10H2
InChIKeyBCZLYNFDOJXWGN-UHFFFAOYSA-N
SMILESN#CC(C=C1)=CC=C1CN2CCOCC2
CAS DataBase Reference37812-51-4
Safety Information
WGK Germany WGK 3
HazardClass IRRITANT
HS Code 29349990
Storage Class11 - Combustible Solids
MSDS Information
4-(Morpholinomethyl)benzonitrile Usage And Synthesis
Chemical Propertieswhite to light yellow crystalline powder
Synthesis
Morpholine

110-91-8

4-Cyanobenzyl bromide

17201-43-3

4-(MORPHOLINOMETHYL)BENZONITRILE

37812-51-4

1. 4-Cyanobenzyl bromide (2.28 g, 11.6 mmol) was dissolved in 25 mL of anhydrous acetonitrile under nitrogen protection. 2. To the above solution, morpholine (1.5 mL, 17.4 mmol) and potassium carbonate (0.69 g, 5 mmol) were added sequentially. 3. Stir the reaction mixture for 30 minutes at room temperature. 4. 4. Upon completion of the reaction, the reaction was quenched with water and extracted with ethyl acetate. 5. The organic layers were combined, dried over anhydrous magnesium sulfate and subsequently concentrated under reduced pressure. 6. 6. The crude product was purified by column chromatography (eluent: hexane-30% ethyl acetate/hexane) to give 4-(4-morpholinylmethyl)benzonitrile. 7. The product was a white solid. 7. The product was a white solid in 96% yield. 8. 8. 1H NMR (400 MHz, CDCl3) δ 7.61 (d, J = 7.9 Hz, 2H), 7.48 (d, J = 8.0 Hz, 2H), 3.71 (s, 4H), 3.55 (s, 2H), 2.44 (s, 4H); 13C NMR (100 MHz, CDCl3): 144.2, 132.5, 129.8, 119.2, 129.8, 119.2 129.8, 119.2, 111.3, 67.2, 63.1, 54.1.

References[1] Journal of Medicinal Chemistry, 2012, vol. 55, # 5, p. 1844 - 1857
[2] Patent: WO2012/69856, 2012, A1. Location in patent: Page/Page column 67
[3] European Journal of Medicinal Chemistry, 2018, vol. 152, p. 31 - 52
[4] Patent: WO2013/153357, 2013, A1. Location in patent: Page/Page column 20; 41; 42
[5] Patent: US2015/45354, 2015, A1. Location in patent: Paragraph 0251-0254
4-(Morpholinomethyl)benzonitrile Preparation Products And Raw materials
Raw materials4-Formylmorpholine-->Morpholine-->4-Cyanobenzyl bromide-->4-(Chloromethyl)tolunitrile-->4-Cyanobenzaldehyde-->Acetonitrile-->Potassium carbonate
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