ChemicalBook--->CAS DataBase List--->112900-82-0

112900-82-0

112900-82-0 Structure

112900-82-0 Structure
IdentificationBack Directory
[Name]

3-Methyl-4-(4-morpholinyl)aniline
[CAS]

112900-82-0
[Synonyms]

3-Methyl-4-morpholinoaniline
3-methyl-4-morpholin-4-ylaniline
3-Methyl-4-(4-morpholinyl)aniline
3-methyl-4-(4-morpholinyl)Benzenamine
Benzenamine, 3-methyl-4-(4-morpholinyl)-
[Molecular Formula]

C11H16N2O
[MDL Number]

MFCD09755865
[MOL File]

112900-82-0.mol
[Molecular Weight]

192.26
Chemical PropertiesBack Directory
[Boiling point ]

373.8±42.0 °C(Predicted)
[density ]

1.122±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
[pka]

7.25±0.40(Predicted)
[Appearance]

Light yellow to brown Solid
Safety DataBack Directory
[HazardClass ]

IRRITANT
[HS Code ]

2934999090
Spectrum DetailBack Directory
[Spectrum Detail]

3-Methyl-4-(4-morpholinyl)aniline(112900-82-0)1HNMR
Hazard InformationBack Directory
[Synthesis]

4-(2-METHYL-4-NITRO-PHENYL)-MORPHOLINE

223404-63-5

3-Methyl-4-(4-morpholinyl)aniline

112900-82-0

General procedure for the synthesis of 3-methyl-4-morpholinoaniline from 4-(2-methyl-4-nitrophenyl)morpholine: a mixture of 4-(2-methyl-4-nitrophenyl)morpholine (6 g, 0.0645 mol, 1.0 eq.) and zinc powder (8.64 g, 0.135 mol, 5 eq.) in methanol (50 mL) in a round-bottomed flask was placed under stirring conditions . Ammonium chloride (7.29 g, 0.135 mol, 5 eq.) was slowly added at 0 °C, followed by stirring the reaction mixture at room temperature for 1 h, during which the progress of the reaction was monitored by thin layer chromatography (TLC). After completion of the reaction, the reaction mixture was filtered through a bed of diatomaceous earth and the filtrate was concentrated under reduced pressure to obtain the residue. The residue was diluted with dichloromethane (DCM, 150 mL) and washed with water. The organic layer was separated, washed with brine solution, dried over anhydrous sodium sulfate, and finally concentrated under reduced pressure to give 3-methyl-4-morpholinoaniline as a brown solid (5 g, 96.35% yield).1H NMR (400 MHz, CDCl3) data: δ 6.768 (d, 1H), 6.39 (s, 1H), 6.36 (d, 1H), 4.66 ( brs, 2H), 3.681 (t, 4H), 2.683 (t, 4H), 2.124 (s, 3H).

[References]

[1] Patent: WO2005/105761, 2005, A1. Location in patent: Page/Page column 36
[2] Journal of Medicinal Chemistry, 2017, vol. 60, # 12, p. 5099 - 5119
[3] Patent: WO2015/38417, 2015, A1. Location in patent: Page/Page column 94; 95
[4] Patent: CN108690043, 2018, A. Location in patent: Paragraph 0262; 0266-0267
[5] Chemical and Pharmaceutical Bulletin, 2001, vol. 49, # 4, p. 353 - 360
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