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4-(Piperidin-4-yl)morpholine

4-(Piperidin-4-yl)morpholine

CAS: 53617-35-9

Molecular Formula: C9H18N2O

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4-(Piperidin-4-yl)morpholine - Names and Identifiers

Name 4-(Piperidin-4-yl)morpholine
Synonyms AKOS BB-9182
CHEMBRDG-BB 4004473
TIMTEC-BB SBB010091
4-Morpholino-piperidin
4-(Piperidin-4-yl)morpholine
4-(PIPERIDIN-4-YL)-MORPHOLINE
4-MORPHOLINO-PIPERDINEDIHYDROCHLORIDE
CAS 53617-35-9
EINECS 627-580-3
InChI InChI=1S/C9H18N2O/c1-3-10-4-2-9(1)11-5-7-12-8-6-11/h9-10H,1-8H2

4-(Piperidin-4-yl)morpholine - Physico-chemical Properties

Molecular FormulaC9H18N2O
Molar Mass170.25
Density1.033±0.06 g/cm3(Predicted)
Melting Point40-43°C(lit.)
Boling Point100-115°C0.15-0.20mm Hg(lit.)
Flash Point>230°F
Vapor Presure0.63-4.58Pa at 25-45℃
AppearanceSolid
pKa10.21±0.10(Predicted)
Storage ConditionKeep in dark place,Sealed in dry,Room Temperature
MDLMFCD03274733

4-(Piperidin-4-yl)morpholine - Risk and Safety

Hazard SymbolsXi - Irritant
Irritant
Risk CodesR36/37/38 - Irritating to eyes, respiratory system and skin.
R20/21/22 - Harmful by inhalation, in contact with skin and if swallowed.
Safety DescriptionS26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36 - Wear suitable protective clothing.
S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection.
WGK Germany3
HS Code29333990
Hazard ClassIRRITANT

4-(Piperidin-4-yl)morpholine - Reference Information

LogP0.3 at 25℃ and pH11
dissociation constant 5.44-10.1 at 20 ℃
Application 4-(4-piperidinyl) morpholine is an organic intermediate, which can be obtained by N-tert-butoxycarbonyl-4-piperidinone and morpholine are reduced and aminated and deprotected. 4-(4-piperidinyl) morpholine can be used to prepare the intermediate 4-{4-ethyl-3-[4-(morpholin-4-yl) piperidin-1-yl] phenyl}-4-methyl-3-oxopentanate tert-butyl ester.
preparation 1) synthesis of compound c16-3: put the compound c16-1(10.0g,50mmol) into a 250mL three-mouth bottle, add anhydrous methanol (100mL), slowly add acetic acid and morpholine (4.78g,55mmol), add palladium carbon (1g.10%), react overnight in hydrogen environment, and the temperament shows that the reaction is complete, spin the solvent, add dichloromethane to dissolve, wash once with a small amount of water, separate the liquid, dry, column chromatography (dichloromethane: methanol = 20:1) to obtain 9g white solid. 2) Synthesis of compound c16-4: Place the compound c16-3(9.0g,33mmol) into a 100mL three-mouth bottle, add 1, 4-dioxane HCl solution, stir, and filter to obtain 9.2g of white solid. The white solid is neutralized with alkali to obtain 4-(4-piperidinyl) morpholine.
Uses 4-(4-piperidinyl) morpholine can be used in biochemical studies to synthesize 2-(4-mercaptoaniline-1-yl)-5-nitrobenzonitrile and 9-bromo-6, 6-dimethyl-8-(4-mercapto-4-yl-piperidin-1-yl)-11-oxo-6,11-Dihydro-5h-benzo (B) cazole-3-carbonylnitrile.
Participate in synthesis:
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Last Update:2024-04-09 20:52:54
4-(Piperidin-4-yl)morpholine
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View History
4-(Piperidin-4-yl)morpholine
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