Product Name

  • Name

    2,3-Dimethyl-2-butene

  • EINECS 209-263-8
  • CAS No. 563-79-1
  • Article Data304
  • CAS DataBase
  • Density 0.697 g/cm3
  • Solubility
  • Melting Point -75 °C
  • Formula C6H12
  • Boiling Point 70.92 °C at 760 mmHg
  • Molecular Weight 84.1613
  • Flash Point 2°F
  • Transport Information UN 3295 3/PG 2
  • Appearance colourless liquid
  • Safety 16-33-62-9
  • Risk Codes 11-65
  • Molecular Structure Molecular Structure of 563-79-1 (2,3-Dimethyl-2-butene)
  • Hazard Symbols FlammableF,HarmfulXn
  • Synonyms 1,1,2,2-Tetramethylethylene;2,3-Dimethyl-2-butene;NSC 73907;Tetramethylethene;Tetramethylethylene;
  • PSA 0.00000
  • LogP 2.36260

Synthetic route

2,3-Dimethyl-1-butene
563-78-0

2,3-Dimethyl-1-butene

2,3-Dimethyl-2-butene
563-79-1

2,3-Dimethyl-2-butene

Conditions
ConditionsYield
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
120-12-7

anthracene

3,3'-bis(3-phenyl-1,1,2,2-tetramethyl-3-silacyclopropane)
188754-05-4

3,3'-bis(3-phenyl-1,1,2,2-tetramethyl-3-silacyclopropane)

A

2,3-Dimethyl-2-butene
563-79-1

2,3-Dimethyl-2-butene

B

3,3,4,4-Tetramethyl-1,2-diphenyl-3,4-dihydro-[1,2]disilete

3,3,4,4-Tetramethyl-1,2-diphenyl-3,4-dihydro-[1,2]disilete

C

C32H32Si2

C32H32Si2

Conditions
ConditionsYield
In benzene at 150℃; for 2h;A 70%
B n/a
C 85%
benzaldehyde
100-52-7

benzaldehyde

acetone
67-64-1

acetone

A

2,3-Dimethyl-2-butene
563-79-1

2,3-Dimethyl-2-butene

B

(2-methyl-1-propenyl)-benzene
768-49-0

(2-methyl-1-propenyl)-benzene

C

stilbene
588-59-0

stilbene

Conditions
ConditionsYield
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
98-86-2

acetophenone

acetone
67-64-1

acetone

A

2,3-Dimethyl-2-butene
563-79-1

2,3-Dimethyl-2-butene

B

α,β,β-trimethylstyrene
769-57-3

α,β,β-trimethylstyrene

C

2,3-diphenyl-2-butene
2510-98-7

2,3-diphenyl-2-butene

Conditions
ConditionsYield
With tin(IV) chloride; zinc In tetrahydrofuran at 64 - 66℃; for 1h; McMurry Reaction; Inert atmosphere;A n/a
B 82%
C n/a
acetone
67-64-1

acetone

2,3-Dimethyl-2-butene
563-79-1

2,3-Dimethyl-2-butene

Conditions
ConditionsYield
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
119-61-9

benzophenone

acetone
67-64-1

acetone

A

2,3-Dimethyl-2-butene
563-79-1

2,3-Dimethyl-2-butene

B

2-methyl-1,1-diphenylpropene
781-33-9

2-methyl-1,1-diphenylpropene

C

1,1,2,2-tetraphenylethylene
632-51-9

1,1,2,2-tetraphenylethylene

Conditions
ConditionsYield
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
55644-09-2

hexamethylsilirane

2,3-Dimethyl-2-butene
563-79-1

2,3-Dimethyl-2-butene

Conditions
ConditionsYield
In benzene at 73℃; for 15h;77%
4,4,5,5-tetramethylethylene sulphate
52393-63-2

4,4,5,5-tetramethylethylene sulphate

2,3-Dimethyl-2-butene
563-79-1

2,3-Dimethyl-2-butene

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 20℃; Product distribution; electrolysis, oth. solvent, var. cathodes;66%
hexamethylsilirane
55644-09-2

hexamethylsilirane

A

2,3-Dimethyl-2-butene
563-79-1

2,3-Dimethyl-2-butene

B

octamethyl-1,2-disilacyclobutane
62346-42-3

octamethyl-1,2-disilacyclobutane

Conditions
ConditionsYield
In benzene at 70℃; for 18h;A 62%
B 38%
2,3-dimethyl-buta-1,3-diene
513-81-5

2,3-dimethyl-buta-1,3-diene

2,3-Dimethyl-2-butene
563-79-1

2,3-Dimethyl-2-butene

Conditions
ConditionsYield
With hydrogen; Et4N60%
With bis(pentamethylcyclopentadienyl)titanium(III) hydride; hydrogen In (2)H8-toluene at 80℃; for 40h; Sealed tube;20%
With diethyl ether; ammonia; sodium
propene
187737-37-7

propene

A

2,3-Dimethyl-2-butene
563-79-1

2,3-Dimethyl-2-butene

B

2-methyl-2-pentene
625-27-4

2-methyl-2-pentene

C

2-Methyl-1-pentene
763-29-1

2-Methyl-1-pentene

D

4-methyl-2-pentene
4461-48-7

4-methyl-2-pentene

E

4-Methyl-1-pentene
691-37-2

4-Methyl-1-pentene

F

2,3-Dimethyl-1-butene
563-78-0

2,3-Dimethyl-1-butene

G

1-hexene 2.2.percent.

1-hexene 2.2.percent.

Conditions
ConditionsYield
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
87050-44-0

(η5-pentamethylcyclopentadienyl)hafnium(2,3-dimethyl-1,3-butadiene)chloride

hydrogen
1333-74-0

hydrogen

A

2,3-Dimethyl-2-butene
563-79-1

2,3-Dimethyl-2-butene

B

tetrakis{(pentamethylcyclopentadienyl)hafnium dihydride chloride}*(toluene)0.5
113180-42-0

tetrakis{(pentamethylcyclopentadienyl)hafnium dihydride chloride}*(toluene)0.5

C

2,3-dimethylbutane
79-29-8

2,3-dimethylbutane

Conditions
ConditionsYield
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
dimesitylfluoroborane
436-59-9

dimesitylfluoroborane

[(HC{C(Me)N-2,6-i-Pr2C6H3}2)Mg(Bpin)(C{N(i-Pr)C(Me)}2)]

[(HC{C(Me)N-2,6-i-Pr2C6H3}2)Mg(Bpin)(C{N(i-Pr)C(Me)}2)]

A

2,3-Dimethyl-2-butene
563-79-1

2,3-Dimethyl-2-butene

B

C24H34B2O2

C24H34B2O2

C

[HC{(Me)CN(2,6-iPr2C6H3)}2Mg{pinB}(DMAP)]

[HC{(Me)CN(2,6-iPr2C6H3)}2Mg{pinB}(DMAP)]

D

[{(HC{C(Me)N-2,6-i-Pr2C6H3}2)Mg}2(F)(O2BC{N(i-Pr)C(Me)}2)]

[{(HC{C(Me)N-2,6-i-Pr2C6H3}2)Mg}2(F)(O2BC{N(i-Pr)C(Me)}2)]

Conditions
ConditionsYield
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
513-81-5

2,3-dimethyl-buta-1,3-diene

A

2,3-Dimethyl-2-butene
563-79-1

2,3-Dimethyl-2-butene

B

2,3-dimethylbutane
79-29-8

2,3-dimethylbutane

C

2,3-Dimethyl-1-butene
563-78-0

2,3-Dimethyl-1-butene

Conditions
ConditionsYield
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;
phenyl isopropyl sulfone
4238-09-9

phenyl isopropyl sulfone

methanesulfonyl chloride
124-63-0

methanesulfonyl chloride

2,3-Dimethyl-2-butene
563-79-1

2,3-Dimethyl-2-butene

Conditions
ConditionsYield
With n-butyllithium In tetrahydrofuran; acetone52%
3,6-Dihydro-4,5-dimethyl-2,2-diphenyl-2H-thiopyran
40754-58-3

3,6-Dihydro-4,5-dimethyl-2,2-diphenyl-2H-thiopyran

A

3,4-dimethylthiophene
632-15-5

3,4-dimethylthiophene

B

2,3-Dimethyl-2-butene
563-79-1

2,3-Dimethyl-2-butene

C

Diphenylmethane
101-81-5

Diphenylmethane

D

3,4-Dimethyl-2-(diphenylmethyl)thiophen
76390-41-5

3,4-Dimethyl-2-(diphenylmethyl)thiophen

Conditions
ConditionsYield
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%

A

3,4-dimethylthiophene
632-15-5

3,4-dimethylthiophene

B

xanthene
92-83-1

xanthene

C

2,3-Dimethyl-2-butene
563-79-1

2,3-Dimethyl-2-butene

D

9H-xanthene-9-thione
492-21-7

9H-xanthene-9-thione

E

9,9'-bixanthene
4381-14-0

9,9'-bixanthene

F

2,3-dimethyl-buta-1,3-diene
513-81-5

2,3-dimethyl-buta-1,3-diene

Conditions
ConditionsYield
at 240 - 260℃; for 0.333333h; Product distribution;A 23 % Spectr.
B 25%
C 8 % Spectr.
D 50%
E 18%
F 26 % Spectr.

A

3,4-dimethylthiophene
632-15-5

3,4-dimethylthiophene

B

thioxanthene
261-31-4

thioxanthene

C

2,3-Dimethyl-2-butene
563-79-1

2,3-Dimethyl-2-butene

D

9,9’-bithioxanthene
10496-86-3

9,9’-bithioxanthene

E

3,4-Dimethyl-2-(9'-thioxanthenyl)thiophen
76390-47-1

3,4-Dimethyl-2-(9'-thioxanthenyl)thiophen

F

2,3-dimethyl-buta-1,3-diene
513-81-5

2,3-dimethyl-buta-1,3-diene

Conditions
ConditionsYield
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}
115982-92-8

tantalum(η5-Cp)(2,3-dimethylbutadiene){C5H6O(isopropyl)2}

A

2,3-Dimethyl-2-butene
563-79-1

2,3-Dimethyl-2-butene

B

2-methyl-3-isopropyl-6-hepten-3-ol
38443-89-9

2-methyl-3-isopropyl-6-hepten-3-ol

C

2,3-Dimethyl-1-butene
563-78-0

2,3-Dimethyl-1-butene

Conditions
ConditionsYield
Hydrolysis of starting compd.; Gas chromy.;A 35%
B 48%
C 17%
dimesitylfluoroborane
436-59-9

dimesitylfluoroborane

[HC{(Me)CN(2,6-iPr2C6H3)}2Mg{pinB}(DMAP)]

[HC{(Me)CN(2,6-iPr2C6H3)}2Mg{pinB}(DMAP)]

A

2,3-Dimethyl-2-butene
563-79-1

2,3-Dimethyl-2-butene

B

C24H34B2O2

C24H34B2O2

C

{(HC{C(Me)N-2,6-i-Pr2C6H3}2)Mg}2(F)(O2BNC5H4-4-NMe2)

{(HC{C(Me)N-2,6-i-Pr2C6H3}2)Mg}2(F)(O2BNC5H4-4-NMe2)

D

C18H22BF*C7H10N2

C18H22BF*C7H10N2

Conditions
ConditionsYield
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
55644-09-2

hexamethylsilirane

A

2,3-Dimethyl-2-butene
563-79-1

2,3-Dimethyl-2-butene

B

Dimethyl-trichloromethyl-(1,1,2-trimethyl-propyl)-silane

Dimethyl-trichloromethyl-(1,1,2-trimethyl-propyl)-silane

C

Chloro-dimethyl-(1,1,2-trimethyl-allyl)-silane

Chloro-dimethyl-(1,1,2-trimethyl-allyl)-silane

D

Dimethyl-trichloromethyl-(1,1,2-trimethyl-allyl)-silane

Dimethyl-trichloromethyl-(1,1,2-trimethyl-allyl)-silane

Conditions
ConditionsYield
With tetrachloromethane In tetrahydrofuran for 1h; Ambient temperature;A n/a
B 19%
C 20%
D 41%
trichlorofluoromethane
75-69-4

trichlorofluoromethane

2,2-dimethoxy-propane
77-76-9

2,2-dimethoxy-propane

A

2,3-Dimethyl-2-butene
563-79-1

2,3-Dimethyl-2-butene

B

isopropyl alcohol
67-63-0

isopropyl alcohol

C

isobutyric Acid
79-31-2

isobutyric Acid

Conditions
ConditionsYield
With lithium aluminium tetrahydride; titanium(IV) iodide In tetrahydrofuran at -5℃; for 0.5h;A 18%
B 12%
C 38%
propene
187737-37-7

propene

A

2,3-Dimethyl-2-butene
563-79-1

2,3-Dimethyl-2-butene

B

2-methyl-2-pentene
625-27-4

2-methyl-2-pentene

C

trans-2-hexene
4050-45-7

trans-2-hexene

D

(E)-4-methylpent-2-ene
674-76-0

(E)-4-methylpent-2-ene

Conditions
ConditionsYield
(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
35913-82-7

cyclopentadienylirondicarbonyl hydride

2,3-dimethyl-buta-1,3-diene
513-81-5

2,3-dimethyl-buta-1,3-diene

A

2,3-Dimethyl-2-butene
563-79-1

2,3-Dimethyl-2-butene

B

cyclopentadienyl iron(II) dicarbonyl dimer
38117-54-3

cyclopentadienyl iron(II) dicarbonyl dimer

C

η5-C5H5Fe(CO)2CH2CMe=CMe2

η5-C5H5Fe(CO)2CH2CMe=CMe2

D

2,3-Dimethyl-1-butene
563-78-0

2,3-Dimethyl-1-butene

Conditions
ConditionsYield
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
594-20-7

2,2-dichloropropane

A

2,3-Dimethyl-2-butene
563-79-1

2,3-Dimethyl-2-butene

B

2-chloropropene
557-98-2

2-chloropropene

C

isopropyl chloride
75-29-6

isopropyl chloride

Conditions
ConditionsYield
With iron pentacarbonyl at 140℃; for 3h; Product distribution; various reaction conditions;A 8%
B 5%
C 16%
d(4)-methanol
811-98-3

d(4)-methanol

3,3,5,5-tetramethyl-3,5-dihydro-4H-pyrazol-4-one
30467-62-0

3,3,5,5-tetramethyl-3,5-dihydro-4H-pyrazol-4-one

A

2,3-Dimethyl-2-butene
563-79-1

2,3-Dimethyl-2-butene

B

C8H12(2)H4O2

C8H12(2)H4O2

C

propan-2-one azine
627-70-3

propan-2-one azine

Conditions
ConditionsYield
at 5℃; for 6h; Irradiation;A 1%
B 11%
C 5%
2-(2,2-dimethylcyclopropyl)acetic acid
68258-20-8

2-(2,2-dimethylcyclopropyl)acetic acid

A

2,3-Dimethyl-2-butene
563-79-1

2,3-Dimethyl-2-butene

B

tert-butylethylene
558-37-2

tert-butylethylene

C

4-Methyl-1-pentene
691-37-2

4-Methyl-1-pentene

D

2,3-Dimethyl-1-butene
563-78-0

2,3-Dimethyl-1-butene

E

CO2

CO2

Conditions
ConditionsYield
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
quinoline
91-22-5

quinoline

2-bromo-2,3-dimethylbutane
594-52-5

2-bromo-2,3-dimethylbutane

2,3-Dimethyl-2-butene
563-79-1

2,3-Dimethyl-2-butene

dimethylketene
598-26-5

dimethylketene

A

2,3-Dimethyl-2-butene
563-79-1

2,3-Dimethyl-2-butene

B

propene
187737-37-7

propene

Conditions
ConditionsYield
With silver at 600 - 700℃; beim Ueberleiten unter vermindertem Druck;
With silver at 600 - 700℃;
phthalic anhydride
85-44-9

phthalic anhydride

3,3-dimethyl-2-butanol
464-07-3, 20281-91-8

3,3-dimethyl-2-butanol

benzenesulfonic acid
98-11-3

benzenesulfonic acid

A

2,3-Dimethyl-2-butene
563-79-1

2,3-Dimethyl-2-butene

B

tert-butylethylene
558-37-2

tert-butylethylene

C

2,3-Dimethyl-1-butene
563-78-0

2,3-Dimethyl-1-butene

2,3-Dimethyl-2-butene Chemical Properties

The molecular structure of 2-Butene, 2,3-dimethyl- (CAS NO.563-79-1) is

IUPAC Name: 2,3-Dimethylbut-2-ene 
Molecular Formula: C6H12
Molecular Weight: 84.16
EINECS: 209-263-8
Density: 0.696 g/cm3
Melting Point: -75 ºC
Boiling Point: 70.9 °C at 760 mmHg
Flash Point: -16 ºC
Freely Rotating Bonds: 0
Polar Surface Area: 0 Å2
Index of Refraction: 1.404
Molar Refractivity: 29.58 cm3
Molar Volume: 120.7 cm3
Polarizability: 11.73 10-24 cm3
Surface Tension: 18.4 dyne/cm 
Enthalpy of Vaporization: 29.64 kJ/mol
Vapour Pressure: 138 mmHg at 25°C 
Stability: stable, highly flammable - readily forms explosive mixtures with air. 
Properties: colourless liquid
The Cas Register Number  of 2-Butene, 2,3-dimethyl- is 563-79-1. The chemical synonyms of 2-Butene, 2,3-dimethyl- (CAS NO.563-79-1) are (CH3)2C=C(CH3)2 ; 1,1,2,2-Tetramethylethylene ; 2,3-dimethyl-2-buten ; 2,3-dimethyl-but-2-ene ; 2,3-Dimethylbut-2-ene ; 2,3-Dimethylbutene-2 ; Tetramethylethene ; Tetramethylethylene . Its  product categories are Acyclic ; Alkenes ; Organic Building Blocks .

2,3-Dimethyl-2-butene Uses

 2-Butene, 2,3-dimethyl- (CAS NO.563-79-1) is used as organic intermediate.

2,3-Dimethyl-2-butene Safety Profile

Hazard Codes: FlammableF,HarmfulXn,CorrosiveC
Risk Statements: 11-65-36/37/38-22-19 
R11: Highly flammable. R65:Harmful: may cause lung damage if swallowed. 
R36/37/38: Irritating to eyes, respiratory system and skin. 
R22: Harmful if swallowed. 
R19: May form explosive peroxides.
Safety Statements: 16-33-62-9-36/37/39-26 
S16: Keep away from sources of ignition. 
S33: Take precautionary measures against static discharges. 
S62: If swallowed, do not induce vomitting; seek medical advice immediately and show this container or label. 
S9: Keep container in a well-ventilated place. 
S36/37/39: Wear suitable protective clothing, gloves and eye/face protection. 
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
RIDADR: UN 3295 3/PG 2
WGK Germany: 3
F: 10-23
Hazard Note: Extremely Flammable/Corrosive/Harmful
HazardClass: 3
PackingGroup: II
HS Code: 29012980

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