ChemicalBook--->CAS DataBase List--->110859-47-7

110859-47-7

110859-47-7 Structure

110859-47-7 Structure
IdentificationMore
[Name]

(4-BENZYL-1,4-OXAZINAN-2-YL)METHYLAMINE
[CAS]

110859-47-7
[Synonyms]

(4-BENZYL-1,4-OXAZINAN-2-YL)METHYLAMINE
(4-BENZYLMORPHOLIN-2-YL) METHANAMINE
(4-BENZYLMORPHOLIN-2-YL)METHYLAMINE
BUTTPARK 85\12-11
C-(4-BENZYL-MORPHOLIN-2-YL)-METHYLAMINE
(4-Benzyl-1,4-oxazinan-2-yl)methylamine 90%
(4-Benzyl-1,4-oxazinan-2-yl)methylamine90%
[Molecular Formula]

C12H18N2O
[MDL Number]

MFCD02682010
[Molecular Weight]

206.28
[MOL File]

110859-47-7.mol
Chemical PropertiesBack Directory
[Boiling point ]

120-122°C 0,5mm
[density ]

1.076
[Fp ]

143℃
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[form ]

solid
[pka]

9.37±0.29(Predicted)
[Appearance]

Colorless to light yellow Viscous Liquid
[Optical Rotation]

0.15°(C=1 g/100ml MEOH)
[CAS DataBase Reference]

110859-47-7(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

R34:Causes burns.
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
[RIDADR ]

2735
[Hazard Note ]

Irritant
[HS Code ]

2921199990
Spectrum DetailBack Directory
[Spectrum Detail]

(4-BENZYL-1,4-OXAZINAN-2-YL)METHYLAMINE(110859-47-7)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

(4-benzyl-1,4-oxazinan-2-yl)methylamine(110859-47-7)
Hazard InformationBack Directory
[Synthesis]

2-(4-BENZYL-MORPHOLIN-2-YLMETHYL)-ISOINDOLE-1,3-DIONE

110859-48-8

(4-BENZYL-1,4-OXAZINAN-2-YL)METHYLAMINE

110859-47-7

General procedure for the synthesis of (4-benzyl-2-morpholinyl)methanamine from 2-[[4-(benzyl)-2-morpholinyl]methyl]-1H-isoindole-1,3(2H)-dione: To a 50 mL single-necked round-bottomed flask was added 2-(4-benzylmorpholin-2-yl)methylphthalimide (1.3 g, 3.87 mmol) and hydrazine hydrate (0.38 g, 7.6 mmol) and ethanol (13 mL) was added. The mixture was heated to 80 °C and then stirred for 4 hours. After completion of the reaction, which was monitored by thin layer chromatography (TLC), the resulting solution was cooled to room temperature and filtered to separate the inorganic material. The filtrate was concentrated under vacuum, 10% sodium hydroxide solution (10 mL) was added and extracted twice with dichloromethane (20 mL). All extracted organic layers were combined, dried with anhydrous magnesium sulfate and filtered. The filtrate was concentrated under vacuum to give a solid product. The resulting solid was dried in an oven at 60 °C to give (4-benzylmorpholin-2-yl)methylamine (550 mg, 69% yield). The dried product was used directly in the subsequent reaction.

[References]

[1] Journal of Medicinal Chemistry, 1990, vol. 33, # 5, p. 1406 - 1413
[2] Journal of Medicinal Chemistry, 1993, vol. 36, # 10, p. 1356 - 1363
[3] Patent: WO2012/128582, 2012, A2. Location in patent: Page/Page column 110
[4] Patent: WO2007/71936, 2007, A1. Location in patent: Page/Page column 86
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