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inquiryMelting point -75 °C Boiling point 73 °C(lit.) density 0.857 g/mL at 25 °C vapor pressure 215 mm Hg ( 37.7 °C) refractive index n20/D 1.412(lit.) Fp 2 °F storage temp. 2-8°C BRN 1361357 Stability: Sta
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Hot Sale 2,3-Dimethyl-2-butene CAS NO.563-79-1 Application:Hot Sale 2,3-Dimethyl-2-butene CAS NO.563-79-1
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inquiryHot Sale 2,3-Dimethyl-2-butene CAS NO.563-79-1Appearance:off-white fine crystalline powder Storage:Dry and ventilated Package:Standard or as customer's require Application:intermediates Transportation:By express (Door to door) such as FEDEX, DHL, EMS
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Hot Sale 2,3-Dimethyl-2-butene CAS NO.563-79-1Appearance:off-white fine crystalline powder Storage:Dry and ventilated Package:Standard or as customer's require Application:intermediates Transportation:Delivery by EMS, DHL, FEDEX, UPS, TNT
Cas:563-79-1
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2-Butene, 2,3-dimethyl- Storage:keep in dry and cool condition Package:25kg or according to cutomer's demand Application:Chemical research/pharma intermediate Transportation:By Sea,by Air,By courier like DHL or Fedx. Port:Shanghai/Shenzhen
Conditions | Yield |
---|---|
aluminum oxide at -0.1℃; for 0.166667h; | 95% |
x In nitromethane at 25℃; for 0.25h; | 88% |
NiX(21) zeolite at -0.1℃; Rate constant; or ZnX(21) zeolite; |
anthracene
3,3'-bis(3-phenyl-1,1,2,2-tetramethyl-3-silacyclopropane)
A
2,3-Dimethyl-2-butene
Conditions | Yield |
---|---|
In benzene at 150℃; for 2h; | A 70% B n/a C 85% |
benzaldehyde
acetone
A
2,3-Dimethyl-2-butene
B
(2-methyl-1-propenyl)-benzene
C
stilbene
Conditions | Yield |
---|---|
With tin(IV) chloride; zinc In tetrahydrofuran at 64 - 66℃; for 1h; McMurry Reaction; Inert atmosphere; | A n/a B 85% C n/a |
acetophenone
acetone
A
2,3-Dimethyl-2-butene
B
α,β,β-trimethylstyrene
C
2,3-diphenyl-2-butene
Conditions | Yield |
---|---|
With tin(IV) chloride; zinc In tetrahydrofuran at 64 - 66℃; for 1h; McMurry Reaction; Inert atmosphere; | A n/a B 82% C n/a |
Conditions | Yield |
---|---|
With tin(IV) chloride; zinc In tetrahydrofuran at 64 - 66℃; McMurry Reaction; Inert atmosphere; | 80% |
With tungsten(VI) chloride In tetrahydrofuran Ambient temperature; electrolysis; | 6% |
With tetrahydrofuran; titanium(II) hydride; magnesium chloride In tetrahydrofuran at -68 - 20℃; | 64 % Chromat. |
benzophenone
acetone
A
2,3-Dimethyl-2-butene
B
2-methyl-1,1-diphenylpropene
C
1,1,2,2-tetraphenylethylene
Conditions | Yield |
---|---|
With tin(IV) chloride; zinc In tetrahydrofuran at 64 - 66℃; for 1h; McMurry Reaction; Inert atmosphere; | A n/a B 80% C n/a |
hexamethylsilirane
2,3-Dimethyl-2-butene
Conditions | Yield |
---|---|
In benzene at 73℃; for 15h; | 77% |
4,4,5,5-tetramethylethylene sulphate
2,3-Dimethyl-2-butene
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 20℃; Product distribution; electrolysis, oth. solvent, var. cathodes; | 66% |
hexamethylsilirane
A
2,3-Dimethyl-2-butene
B
octamethyl-1,2-disilacyclobutane
Conditions | Yield |
---|---|
In benzene at 70℃; for 18h; | A 62% B 38% |
Conditions | Yield |
---|---|
With hydrogen; Et4N | 60% |
With bis(pentamethylcyclopentadienyl)titanium(III) hydride; hydrogen In (2)H8-toluene at 80℃; for 40h; Sealed tube; | 20% |
With diethyl ether; ammonia; sodium |
propene
A
2,3-Dimethyl-2-butene
B
2-methyl-2-pentene
C
2-Methyl-1-pentene
D
4-methyl-2-pentene
E
4-Methyl-1-pentene
F
2,3-Dimethyl-1-butene
Conditions | Yield |
---|---|
diethylaluminium chloride In benzene at 50℃; under 6840 Torr; for 2h; Product distribution; 0 - 60 deg C, 1 - 32 h, influence of the catalysts on the yields; | A 5.4% B 3.2% C 18.4% D 58.2% E 10.2% F 2.1% G n/a |
(η5-pentamethylcyclopentadienyl)hafnium(2,3-dimethyl-1,3-butadiene)chloride
hydrogen
A
2,3-Dimethyl-2-butene
B
tetrakis{(pentamethylcyclopentadienyl)hafnium dihydride chloride}*(toluene)0.5
C
2,3-dimethylbutane
Conditions | Yield |
---|---|
In toluene A pressure vessel is filled with a soln. of (C5Me5)Hf(C6H10)Cl in toluene and charged with 10 atm of H2, reaction mixture is stirred overnight at 70°C under N2.; Excess H2 is released, hot soln. is transferred into a Schlenk vessel, cooling of the soln. to room temp., a bright yellow ppt. is formed, solvent is decanted, ppt. is redissolved (hot toluene), slow cooling to -30°C, elem. anal.; | A n/a B 56% C n/a |
Conditions | Yield |
---|---|
In (2)H8-toluene at 20℃; for 1h; Schlenk technique; Inert atmosphere; Glovebox; | A n/a B n/a C n/a D 53% |
2,3-dimethyl-buta-1,3-diene
A
2,3-Dimethyl-2-butene
B
2,3-dimethylbutane
C
2,3-Dimethyl-1-butene
Conditions | Yield |
---|---|
With hydrogen; palladium dichloride In N,N-dimethyl-formamide under 18751.5 Torr; for 0.25h; Product distribution; Ambient temperature; various time; | A 39.3% B 0.05% C 52.2% |
With hydrogen; 1,5-hexadienerhodium(I)-chloride dimer In various solvent(s) for 2h; Ambient temperature; pH=7.6; | A 27% B 25% C 22% |
With bis(1,5-cyclooctadiene)rhodium(I) tetrafluoroborate; hydrogen; disodium salt of the bis(m-sulfonatophenyl)-n-butylphosphane at 60℃; under 22502.3 Torr; for 6h; Ionic liquid; chemoselective reaction; |
Conditions | Yield |
---|---|
With n-butyllithium In tetrahydrofuran; acetone | 52% |
3,6-Dihydro-4,5-dimethyl-2,2-diphenyl-2H-thiopyran
A
3,4-dimethylthiophene
B
2,3-Dimethyl-2-butene
C
Diphenylmethane
D
3,4-Dimethyl-2-(diphenylmethyl)thiophen
Conditions | Yield |
---|---|
at 240 - 260℃; for 0.333333h; Product distribution; | A 4 % Spectr. B 8 % Spectr. C 48% D 50% |
at 240 - 260℃; for 0.333333h; | A 4 % Spectr. B 8 % Spectr. C 48% D 50% |
Spiro
A
3,4-dimethylthiophene
B
xanthene
C
2,3-Dimethyl-2-butene
D
9H-xanthene-9-thione
E
9,9'-bixanthene
F
2,3-dimethyl-buta-1,3-diene
Conditions | Yield |
---|---|
at 240 - 260℃; for 0.333333h; Product distribution; | A 23 % Spectr. B 25% C 8 % Spectr. D 50% E 18% F 26 % Spectr. |
Spiro
A
3,4-dimethylthiophene
B
thioxanthene
C
2,3-Dimethyl-2-butene
D
9,9’-bithioxanthene
E
3,4-Dimethyl-2-(9'-thioxanthenyl)thiophen
F
2,3-dimethyl-buta-1,3-diene
Conditions | Yield |
---|---|
at 240 - 260℃; for 0.333333h; Product distribution; | A 35 % Spectr. B 48% C 7 % Spectr. D 10% E 11% F 7 % Spectr. |
tantalum(η5-Cp)(2,3-dimethylbutadiene){C5H6O(isopropyl)2}
A
2,3-Dimethyl-2-butene
B
2-methyl-3-isopropyl-6-hepten-3-ol
C
2,3-Dimethyl-1-butene
Conditions | Yield |
---|---|
Hydrolysis of starting compd.; Gas chromy.; | A 35% B 48% C 17% |
Conditions | Yield |
---|---|
In (2)H8-toluene at 60℃; for 5h; Schlenk technique; Glovebox; Inert atmosphere; | A n/a B n/a C 48% D n/a |
hexamethylsilirane
A
2,3-Dimethyl-2-butene
Conditions | Yield |
---|---|
With tetrachloromethane In tetrahydrofuran for 1h; Ambient temperature; | A n/a B 19% C 20% D 41% |
trichlorofluoromethane
2,2-dimethoxy-propane
A
2,3-Dimethyl-2-butene
B
isopropyl alcohol
C
isobutyric Acid
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride; titanium(IV) iodide In tetrahydrofuran at -5℃; for 0.5h; | A 18% B 12% C 38% |
propene
A
2,3-Dimethyl-2-butene
B
2-methyl-2-pentene
C
trans-2-hexene
D
(E)-4-methylpent-2-ene
Conditions | Yield |
---|---|
(C3H5)2AlCl; Ni(C6H7O2)2; triphenylphosphine Further byproducts given. Title compound not separated from byproducts; | A 2% B 25% C 16% D 17.7% |
cyclopentadienylirondicarbonyl hydride
2,3-dimethyl-buta-1,3-diene
A
2,3-Dimethyl-2-butene
B
cyclopentadienyl iron(II) dicarbonyl dimer
D
2,3-Dimethyl-1-butene
Conditions | Yield |
---|---|
In pentane under N2, stirring at room temp, the react. was complete within about 1 h; evapn. (vac.), chromy. on alumina (eluent pentane for the hydrometalated products, and more polar solvents for the dimer), elem. anal., (the org. products identified by GC and NMR); | A n/a B 20% C 8% D n/a |
2,2-dichloropropane
A
2,3-Dimethyl-2-butene
B
2-chloropropene
C
isopropyl chloride
Conditions | Yield |
---|---|
With iron pentacarbonyl at 140℃; for 3h; Product distribution; various reaction conditions; | A 8% B 5% C 16% |
d(4)-methanol
3,3,5,5-tetramethyl-3,5-dihydro-4H-pyrazol-4-one
A
2,3-Dimethyl-2-butene
C
propan-2-one azine
Conditions | Yield |
---|---|
at 5℃; for 6h; Irradiation; | A 1% B 11% C 5% |
2-(2,2-dimethylcyclopropyl)acetic acid
A
2,3-Dimethyl-2-butene
B
tert-butylethylene
C
4-Methyl-1-pentene
D
2,3-Dimethyl-1-butene
Conditions | Yield |
---|---|
at 496.9℃; for 0.25h; Product distribution; Thermodynamic data; Rate constant; | A 11% B n/a C n/a D n/a E n/a |
Conditions | Yield |
---|---|
With silver at 600 - 700℃; beim Ueberleiten unter vermindertem Druck; | |
With silver at 600 - 700℃; |
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