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inquiryProduct Name 2-Methyl-1-[4-(methylthio)phenyl]-2-morpholinopropanone-1 CAS No. 71868-10-5 Molecular Formula
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inquiry■POLYMER ADDITIVES JADEWIN PI907 PHOTO INITIATOR CHEMICAL COMPONENT COMPONENT 2-Methyl-4'-(methylthio)-2-morpholinopropiophenone CAS 71868-10-5 Molecular C15H21NO2S M.W 279 SPECIFICATION
morpholine
2-methyl-1-[4-(methylthio)phenyl]-2-morpholinopropan-1-one
Conditions | Yield |
---|---|
With calcium hydroxide at 20 - 138℃; for 20h; | 90.2% |
With tetra(n-butyl)ammonium hydrogensulfate; sodium hydroxide for 8h; Reflux; | 43% |
at 105 - 110℃; for 20h; Temperature; | 119.3 g |
at 105 - 115℃; for 20h; | 112.57 g |
With water at 105℃; for 12h; Reagent/catalyst; Large scale; |
1-methoxy-4-methylsulfanyl-benzene
2-methyl-1-[4-(methylthio)phenyl]-2-morpholinopropan-1-one
Conditions | Yield |
---|---|
With bis(1,5-cyclooctadiene)nickel (0); 1,2-bis-(dicyclohexylphosphino)ethane In o-xylene at 140℃; for 24h; Glovebox; Inert atmosphere; | 74% |
morpholine
2-methyl-1-(4-(methylthio)phenyl)-propan-1-one
2-methyl-1-[4-(methylthio)phenyl]-2-morpholinopropan-1-one
Conditions | Yield |
---|---|
Stage #1: 2-methyl-1-(4-(methylthio)phenyl)-propan-1-one With hexachloroethane; sodium methylate In methanol at 40℃; for 24h; Stage #2: morpholine With tetra(n-butyl)ammonium hydrogensulfate; sodium hydroxide for 10h; Reagent/catalyst; Temperature; Reflux; | 61% |
morpholine
2-bromo-2-methyl-1-[4-(methylsulfanyl)phenyl]propan-1-one
2-methyl-1-[4-(methylthio)phenyl]-2-morpholinopropan-1-one
Conditions | Yield |
---|---|
Stage #1: morpholine With aluminum (III) chloride In 1,2-dichloro-ethane at 40℃; for 0.5h; Stage #2: 2-bromo-2-methyl-1-[4-(methylsulfanyl)phenyl]propan-1-one In 1,2-dichloro-ethane at 40℃; for 6h; | 60.57% |
2-methyl-1-(4-(methylthio)phenyl)-propan-1-one
2-methyl-1-[4-(methylthio)phenyl]-2-morpholinopropan-1-one
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: bromine / 2 h / 20 - 30 °C 2.1: aluminum (III) chloride / 1,2-dichloro-ethane / 0.5 h / 40 °C 2.2: 6 h / 40 °C View Scheme | |
Multi-step reaction with 3 steps 1: bromine / 2 h / 20 - 30 °C 2: 1 h / 20 °C 3: 20 h / 105 - 115 °C View Scheme | |
Multi-step reaction with 2 steps 1: hexachloroethane / 20 °C 2: sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate / 8 h / Reflux View Scheme |
methyl-phenyl-thioether
2-methyl-1-[4-(methylthio)phenyl]-2-morpholinopropan-1-one
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1.1: aluminum (III) chloride / dichloromethane / 7.5 h / 15 - 35 °C 2.1: bromine / 2 h / 20 - 30 °C 3.1: aluminum (III) chloride / 1,2-dichloro-ethane / 0.5 h / 40 °C 3.2: 6 h / 40 °C View Scheme | |
Multi-step reaction with 4 steps 1: aluminum (III) chloride / dichloromethane / 7.5 h / 15 - 35 °C 2: bromine / 2 h / 20 - 30 °C 3: 1 h / 20 °C 4: 20 h / 105 - 115 °C View Scheme |
2-methyl-1-[4-(methylthio)phenyl]-2-morpholinopropan-1-one
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: methanol / 1 h / 20 °C 2: 20 h / 105 - 115 °C View Scheme |
2-bromo-2-methyl-1-[4-(methylsulfanyl)phenyl]propan-1-one
2-methyl-1-[4-(methylthio)phenyl]-2-morpholinopropan-1-one
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: morpholine; sodium methylate / 28 - 85 °C / 760.05 Torr / Large scale 2: water / 12 h / 105 °C / Large scale View Scheme |
terephthalonitrile
2-methyl-1-[4-(methylthio)phenyl]-2-morpholinopropan-1-one
Conditions | Yield |
---|---|
With bis(1,5-cyclooctadiene)nickel (0); 1,2-bis-(dicyclohexylphosphino)ethane In o-xylene at 140℃; for 24h; Glovebox; Inert atmosphere; | 94% |
2-methyl-1-[4-(methylthio)phenyl]-2-morpholinopropan-1-one
Cyclohexanethiol
Conditions | Yield |
---|---|
With bis(1,5-cyclooctadiene)nickel (0); lithium hexamethyldisilazane; 1,2-bis-(dicyclohexylphosphino)ethane In toluene at 100℃; for 12h; Glovebox; Inert atmosphere; | 91% |
2-methyl-1-[4-(methylthio)phenyl]-2-morpholinopropan-1-one
bromoacetic acid methyl ester
methyl 2-((4-(2-methyl-2-morpholinopropanoyl)phenyl)thio)acetate
Conditions | Yield |
---|---|
In 2,2,2-trifluoroethanol at 100℃; for 24h; | 89% |
Conditions | Yield |
---|---|
With bis(1,5-cyclooctadiene)nickel (0); lithium hexamethyldisilazane; 1,2-bis-(dicyclohexylphosphino)ethane In toluene at 100℃; for 12h; Buchwald-Hartwig Coupling; | 68% |
2-methyl-1-[4-(methylthio)phenyl]-2-morpholinopropan-1-one
A
2-morpholino propan-2-yl radical
B
C8H7OS
Conditions | Yield |
---|---|
In various solvent(s) at -40.1℃; Irradiation; Title compound not separated from byproducts; | |
In acetonitrile UV-irradiation; |
2-methyl-1-[4-(methylthio)phenyl]-2-morpholinopropan-1-one
dicyclohexyl itaconate
poly(dicyclohexyl itaconate) dimethyl(morpholino)methyl-terminated; monomer(s): dicyclohexyl itaconate; 2-methyl-1-[4-(methylthio)phenyl]-2-morpholinopropan-1-one
Conditions | Yield |
---|---|
at 20℃; pulsed lazer irradiation; |
2-methyl-1-[4-(methylthio)phenyl]-2-morpholinopropan-1-one
acrylic acid methyl ester
poly(methyl acrylate), p-methylthiobenzoyl- and dimethyl(morpholino)methyl-terminated; monomer(s): methyl acrylate; 2-methyl-1-[4-(methylthio)phenyl]-2-morpholinopropan-1-one
Conditions | Yield |
---|---|
at -34℃; pulsed lazer irradiation; |
2-methyl-1-[4-(methylthio)phenyl]-2-morpholinopropan-1-one
Conditions | Yield |
---|---|
at 70℃; UV-irradiation; |
2-methyl-1-[4-(methylthio)phenyl]-2-morpholinopropan-1-one
dimethyl sulfate
Conditions | Yield |
---|---|
In water; acetonitrile at 25 - 60℃; |
2-methyl-1-[4-(methylthio)phenyl]-2-morpholinopropan-1-one
Conditions | Yield |
---|---|
Stage #1: 2-methyl-1-[4-(methylthio)phenyl]-2-morpholinopropan-1-one With 3-chloro-benzenecarboperoxoic acid In dichloromethane for 2.5h; Cooling with ice; Stage #2: With sodium hydroxide In dichloromethane; water |
2-methyl-1-[4-(methylthio)phenyl]-2-morpholinopropan-1-one
Conditions | Yield |
---|---|
With tetrafluoroboric acid In diethyl ether for 2h; Cooling with ice; |
2-methyl-1-[4-(methylthio)phenyl]-2-morpholinopropan-1-one
dimethyl-[4-(2-methyl-2-morpholino-propanoyl)phenyl]sulfonium methyl sulfate
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: acetonitrile; water / 25 - 60 °C 2: sodium hydroxide; sodium carbonate / water / 0.5 h / 25 °C / pH 9 View Scheme |
2-methyl-1-[4-(methylthio)phenyl]-2-morpholinopropan-1-one
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: acetonitrile; water / 25 - 60 °C 2: sodium hexaflorophosphate; sodium carbonate / water / pH 9.2 View Scheme |
2-methyl-1-[4-(methylthio)phenyl]-2-morpholinopropan-1-one
2-methyl-1-(4-methylsulfanylphenyl)-2-morpholin-4-ium-4-yl-propan-1-one chloride
Conditions | Yield |
---|---|
With hydrogenchloride In propan-1-ol; water for 1h; |
2-methyl-1-[4-(methylthio)phenyl]-2-morpholinopropan-1-one
triethyloxonium fluoroborate
Conditions | Yield |
---|---|
In dichloromethane at 25℃; for 5h; | 90 %Spectr. |
2-methyl-1-[4-(methylthio)phenyl]-2-morpholinopropan-1-one
Conditions | Yield |
---|---|
With sulfuryl dichloride In 1,2-dichloro-ethane at 20 - 30℃; for 4h; Reagent/catalyst; Temperature; Overall yield = 16.5 g; |
2-methyl-1-[4-(methylthio)phenyl]-2-morpholinopropan-1-one
Conditions | Yield |
---|---|
Stage #1: 2-methyl-1-[4-(methylthio)phenyl]-2-morpholinopropan-1-one With sulfuryl dichloride In 1,2-dichloro-ethane for 1h; Stage #2: With carbonic acid dimethyl ester; sodium hydroxide In methanol for 6.25h; Inert atmosphere; Reflux; | 8.5 g |
2-methyl-1-[4-(methylthio)phenyl]-2-morpholinopropan-1-one
1-chloroacetophenone
Conditions | Yield |
---|---|
In acetone for 2h; Inert atmosphere; |
2-methyl-1-[4-(methylthio)phenyl]-2-morpholinopropan-1-one
1-chloroacetophenone
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: acetone / 2 h / Inert atmosphere 2: potassium hexafluorophosphate / acetone / 2 h / Heating View Scheme |
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