Conditions | Yield |
---|---|
With potassium hydroxide; Pd/C; zinc(II) oxide at 200℃; for 15h; | 76% |
2,6-Di-tert-butyl-4-(1-hydroxyethyl)phenol
2,6-di-tert-butyl-4-ethylphenol
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In tetrahydrofuran; chlorobenzene for 1h; Heating; | 70% |
5,7-di-t-butylspiro[2.5]octa-4,7-dien-6-one
A
2,6-di-tert-butyl-4-ethylphenol
B
1,4-bis-(3,5-di-tert-butyl-4-oxyphenyl)butane
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide for 0.616667h; electrolysis, n-Bu4NClO4; | A 43% B 28% |
2,6-di-tert-butylphenol
paracetaldehyde
A
2,6-di-tert-butyl-4-ethylphenol
B
1,3-bis(3,5-di-tert-butyl-4-hydroxyphenyl)butane
C
2,4-di-tert-Butylphenol
D
3-(3,5-di-tert-butyl-4-hydroxyphenyl)butan-1-ol
Conditions | Yield |
---|---|
With potassium hydroxide In ethanol at 230℃; for 0.333333h; | A n/a B 8% C 2% D 11.3% |
Conditions | Yield |
---|---|
With sodium hydroxide; ethanol at 225℃; |
4-Ethylphenol
isobutene
A
2,6-di-tert-butyl-4-ethylphenol
B
6-di-t-butyl-4-ethylphenol
Conditions | Yield |
---|---|
With sulfuric acid | |
With sulfuric acid at 70℃; |
2,6-di-tert-butylphenol
ethyl iodide
A
2,6-di-tert-butyl-4-ethylphenol
B
1,3-di-tert-butyl-2-ethoxybenzene
C
2,6-Di-tert-butyl-4-aethyl-phenetol
D
2,6-Di-tert.-butyl-4,4-diethyl-cyclohexadien-(2,5)-on-(1)
Conditions | Yield |
---|---|
(i) KOtBu, tBuOH, (ii) NaH, PE; Multistep reaction. Further byproducts given; |
2,6-Di-tert-butyl-4-(1-hydroxyethyl)phenol
A
2,6-di-tert-butyl-4-ethylphenol
B
1-(3,5-di-tert-butyl-4-hydroxyphenyl)ethanone
Conditions | Yield |
---|---|
aluminum oxide under 5 Torr; Heating; Yield given. Yields of byproduct given; |
4-Aethyl-2,6-di-tert-butyl-phenoxyl-Radikal
A
2,6-di-tert-butyl-4-ethylphenol
B
2,6-di-tert-butyl-4-ethylidenecyclohexa-2,5-en-1-one
Conditions | Yield |
---|---|
Rate constant; Thermodynamic data; rate constant of the disproportionation; |
4-ethyl-2,6-di-tert-butyl-4-hydroxy-2,5-cyclohexadienone
A
2,6-di-tert-butyl-4-ethylphenol
Conditions | Yield |
---|---|
With sodium hydroxide; sodium tetrahydroborate In methanol at 30℃; for 48h; Yield given. Yields of byproduct given; |
4-Ethylphenol
sulfuric acid
isobutene
A
2,6-di-tert-butyl-4-ethylphenol
B
6-di-t-butyl-4-ethylphenol
2,6-di-tert-butylphenol
crotonaldehyde
A
2,6-di-tert-butyl-4-ethylphenol
B
1,3-bis(3,5-di-tert-butyl-4-hydroxyphenyl)butane
C
4,4'-Methylenebis(2,6-di-tert-butylphenol)
D
1,1-bis(3,5-di-tert-butyl-4-hydroxyphenyl)ethane
E
3-(3,5-di-tert-butyl-4-hydroxyphenyl)butan-1-ol
Conditions | Yield |
---|---|
With potassium hydroxide In ethanol at 230℃; for 0.5h; | A 10 g B n/a C n/a D n/a E 3 g |
2,6-di-tert-butylphenol
2,2'-[1,2-ethanediylbis(oxy)]bisethanol
A
2,6-di-tert-butyl-4-ethylphenol
B
2,6-di-tert-butyl-4-propyllphenol
C
1,2-bis(2,6-di-tert-butyl-4-hydroxyphenyl)ethane
E
2,6-di-tert-butyl-4-methyl-phenol
F
2,6-di-tert-butyl-4-isopropylphenol
G
2-(3,5-di-t-butyl-4-hydroxyphenyl)ethanol
H
ethylene glycol 2-(3,5-di-tert-butyl-4-hydroxyphenyl)-ethyl ether
I
6-di-t-butyl-4-ethylphenol
J
4-butyl-2,6-di-tert-butylphenol
Conditions | Yield |
---|---|
With sodium hydroxide at 220℃; for 5h; |
4-methoxy-phenol
A
4-Ethylphenol
B
2,6-di-tert-butylphenol
C
3-ethylphenol
D
2,4-diisopropylphenol
E
2,6-diisopropylphenol
F
3,5-diisopropylphenol
G
2,4,6-triisopropylphenol
H
2,6-di-tert-butyl-4-ethylphenol
I
2,4-di-tert-Butylphenol
J
3,5-diethylphenol
K
2,4-diethylphenol
L
2,4-di-tert-amylphenol
M
2,5-diethyl phenol
N
2,5-di-(sec-butyl)phenol
Conditions | Yield |
---|---|
With molybdenum(VI) oxide In ethanol at 280℃; for 4h; Inert atmosphere; |
2-Ethoxyphenol
B
4-Ethylphenol
C
2,6-di-tert-butylphenol
D
3-ethylphenol
E
2,4-diisopropylphenol
F
Durohydroquinone
G
2,6-diisopropylphenol
H
2,6-di-tert-butyl-4-ethylphenol
I
3,5-Di-tert-butylphenol
J
3,5-diethylphenol
K
2,5-di-tert-butylphenol
L
2,5-Diisopropylphenol
M
2,5-diethyl phenol
Conditions | Yield |
---|---|
With molybdenum(VI) oxide In ethanol at 280℃; for 4h; Inert atmosphere; |
benzene-1,2-diol
A
2,6-di-tert-butylphenol
B
2,4-diisopropylphenol
C
2,6-diisopropylphenol
D
2,4,6-triisopropylphenol
E
2,6-di-tert-butyl-4-ethylphenol
F
3,5-diethylphenol
G
2,5-di-tert-butylphenol
H
2,5-diethyl phenol
I
2,5-di-(sec-butyl)phenol
Conditions | Yield |
---|---|
With molybdenum(VI) oxide In ethanol at 280℃; for 4h; Inert atmosphere; |
2-methoxy-phenol
A
o-Hydroxyethylbenzene
B
2,6-di-tert-butylphenol
C
2,4-diisopropylphenol
D
2,6-diisopropylphenol
E
2,4,6-triisopropylphenol
F
2,6-di-tert-butyl-4-ethylphenol
G
2,4-di-tert-Butylphenol
H
3,5-diethylphenol
I
2,4-di-tert-amylphenol
J
2,5-diethyl phenol
K
2,5-di-(sec-butyl)phenol
Conditions | Yield |
---|---|
With molybdenum(VI) oxide In ethanol at 280℃; for 4h; Catalytic behavior; Temperature; Solvent; Time; Reagent/catalyst; Inert atmosphere; |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: water; methanol / 3 h / 90 °C 2: palladium; hydrogen / 4 h / 140 °C View Scheme |
N,N-dimethyl-2-(3,5-di-tert-butyl-4-hydroxyphenyl)ethylamine
2,6-di-tert-butyl-4-ethylphenol
Conditions | Yield |
---|---|
With hydrogen; palladium at 140℃; for 4h; | 225.37 g |
ethanol
2-methoxy-phenol
A
3,5-Di-tert-butylcatechol
B
2,6-di-tert-butylphenol
C
2,4-diisopropylphenol
D
2,6-diisopropylphenol
E
2,4,6-triisopropylphenol
F
2,6-di-tert-butyl-4-ethylphenol
G
2,6-di-tert-butyl-4-hydroxyphenol
H
2,6-di-tert-butyl-4-methoxymethylene-phenol
I
3,5-Di-tert-butylphenol
J
2,4-dimethyl-6-tert-butylphenol
K
2-(2',5'-dimethoxyphenyl)propionaldehyde
L
2,6-di-tert-butyl-4-sec-butylphenol
M
1,2-diethoxybenzene
N
1,4-dimethoxy-2-tert-butylbenzene
O
1-ethoxy-4-methoxybenzene
P
2,5-di(tert-amyl)-1,4-hydroquinone
Q
2,4-di-tert-amylphenol
R
2,5-diethyl phenol
S
4-ethoxy-3-methoxytoluene
T
1,2-dimethoxy-4-butylbenzene
U
1,2-diethoxy-4-ethyl-benzene
V
3,5-di-t-butyl-4-hydroxybenzaldehyde
Conditions | Yield |
---|---|
With ortho-tungstic acid at 300℃; for 6h; Autoclave; |
ethanol
2-methoxy-phenol
A
2-Ethoxyphenol
B
3,5-Di-tert-butylcatechol
C
2,4-diisopropylphenol
D
2,6-diisopropylphenol
E
2,4,6-triisopropylphenol
F
2,6-di-tert-butyl-4-ethylphenol
G
2,6-di-tert-butyl-4-hydroxyphenol
H
2,6-di-tert-butyl-4-methoxymethylene-phenol
I
3,5-Di-tert-butylphenol
J
2,4-dimethyl-6-tert-butylphenol
K
2-(2',5'-dimethoxyphenyl)propionaldehyde
L
2,6-di-tert-butyl-4-sec-butylphenol
M
1,2-diethoxybenzene
N
1,4-dimethoxy-2-tert-butylbenzene
O
1-ethoxy-4-methoxybenzene
P
2,5-di(tert-amyl)-1,4-hydroquinone
Q
2,4-di-tert-amylphenol
R
2,5-diethyl phenol
S
4-ethoxy-3-methoxytoluene
T
1,2-dimethoxy-4-butylbenzene
U
1,2-diethoxy-4-ethyl-benzene
V
3,5-di-t-butyl-4-hydroxybenzaldehyde
Conditions | Yield |
---|---|
With tungsten(VI) oxide at 300℃; for 6h; Reagent/catalyst; Autoclave; |
ethanol
benzene-1,2-diol
A
3,5-Di-tert-butylcatechol
B
2,6-di-tert-butylphenol
C
2,4-diisopropylphenol
D
2,6-diisopropylphenol
E
2,4,6-triisopropylphenol
F
2,6-di-tert-butyl-4-ethylphenol
G
2,6-di-tert-butyl-4-hydroxyphenol
H
2,6-di-tert-butyl-4-methoxymethylene-phenol
I
3,5-Di-tert-butylphenol
J
2,4-dimethyl-6-tert-butylphenol
K
2-(2',5'-dimethoxyphenyl)propionaldehyde
L
2,6-di-tert-butyl-4-sec-butylphenol
M
1,2-diethoxybenzene
N
1,4-dimethoxy-2-tert-butylbenzene
O
1-ethoxy-4-methoxybenzene
P
2,5-di(tert-amyl)-1,4-hydroquinone
Q
2,4-di-tert-amylphenol
R
2,5-diethyl phenol
S
4-ethoxy-3-methoxytoluene
T
1,2-dimethoxy-4-butylbenzene
U
1,2-diethoxy-4-ethyl-benzene
V
3,5-di-t-butyl-4-hydroxybenzaldehyde
Conditions | Yield |
---|---|
With ortho-tungstic acid at 300℃; for 6h; Autoclave; |
2-Ethoxyphenol
ethanol
A
3,5-Di-tert-butylcatechol
B
2,6-di-tert-butylphenol
C
2,4-diisopropylphenol
D
2,6-diisopropylphenol
E
2,4,6-triisopropylphenol
F
2,6-di-tert-butyl-4-ethylphenol
G
2,6-di-tert-butyl-4-hydroxyphenol
H
2,6-di-tert-butyl-4-methoxymethylene-phenol
I
3,5-Di-tert-butylphenol
J
2,4-dimethyl-6-tert-butylphenol
K
2-(2',5'-dimethoxyphenyl)propionaldehyde
L
2,6-di-tert-butyl-4-sec-butylphenol
M
1,2-diethoxybenzene
N
1,4-dimethoxy-2-tert-butylbenzene
O
1-ethoxy-4-methoxybenzene
P
2,5-di(tert-amyl)-1,4-hydroquinone
Q
2,4-di-tert-amylphenol
R
2,5-diethyl phenol
S
4-ethoxy-3-methoxytoluene
T
1,2-dimethoxy-4-butylbenzene
U
1,2-diethoxy-4-ethyl-benzene
V
3,5-di-t-butyl-4-hydroxybenzaldehyde
Conditions | Yield |
---|---|
With ortho-tungstic acid at 300℃; for 6h; Autoclave; |
ethanol
2-methoxy-phenol
A
o-Hydroxyethylbenzene
B
2,6-di-tert-butylphenol
C
3-ethylphenol
D
2,4-diisopropylphenol
E
2,6-diisopropylphenol
F
2,6-di-tert-butyl-4-ethylphenol
G
1,4-diethylbenzene
H
3,5-diethylphenol
I
2,5-di-tert-butylphenol
J
1,3,5-triethylbenzene
K
4-Ethylguaiacol
L
2,5-diethyl phenol
M
2,4-diisopropyl-5-methylphenol
N
1-(2,4,5-triethylphenyl)ethanone
O
1-ethyl-3-tert-butyl-5-methyl-benzene
P
methoxybenzene
Q
phenol
Conditions | Yield |
---|---|
With perrhenic acid anhydride at 320℃; for 6h; Inert atmosphere; Sealed tube; |
2,6-di-tert-butyl-4-ethylphenol
4-ethyl-2,6-di-tert-butyl-4-hydroxy-2,5-cyclohexadienone
Conditions | Yield |
---|---|
With cesium hydroxide; oxygen; triethyl phosphite In dimethyl sulfoxide at 25℃; under 760.051 Torr; for 12h; | 96% |
With perchloric acid; water; lead dioxide In acetone for 0.133333h; | 83% |
With potassium tert-butylate; oxygen |
2,6-di-tert-butyl-4-ethylphenol
2,6-di-tert-butyl-4-ethyl-4-hydroperoxycyclohexa-2,5-dienone
Conditions | Yield |
---|---|
With 2,8-dibromo-5,5-difluoro-1,3,7,9-tetramethyl-10-phenyl-5H-dipyrrolo[1,2-c:2′,1′-f ][1,3,2]diazaborinin-4-ium-5-uide; oxygen In 1,4-dioxane for 6h; Irradiation; | 96% |
With potassium hydroxide; oxygen In ethanol; water | 70% |
With potassium hydroxide; oxygen In ethanol at 0 - 5℃; for 14h; |
Conditions | Yield |
---|---|
With copper(l) iodide; 1,8-diazabicyclo[5.4.0]undec-7-ene; 4,4'-di-tert-butyl-2,2'-bipyridine In toluene at 20℃; for 1h; Solvent; Reagent/catalyst; Temperature; Inert atmosphere; | 96% |
2,6-di-tert-butyl-4-ethylphenol
Conditions | Yield |
---|---|
With copper(l) iodide; 1,8-diazabicyclo[5.4.0]undec-7-ene; 4,4'-di-tert-butyl-2,2'-bipyridine In toluene at 20℃; for 1h; Inert atmosphere; | 91% |
2,6-di-tert-butyl-4-ethylphenol
Conditions | Yield |
---|---|
With nitrogen(II) oxide; sodium In methanol at 20℃; under 1810.07 Torr; for 24h; Addition; | 88% |
Conditions | Yield |
---|---|
With perchloric acid; lead dioxide for 0.133333h; | 88% |
2,6-di-tert-butyl-4-ethylphenol
Conditions | Yield |
---|---|
With copper(l) iodide; 1,8-diazabicyclo[5.4.0]undec-7-ene; 4,4'-di-tert-butyl-2,2'-bipyridine In toluene at 20℃; for 20h; Inert atmosphere; | 88% |
2,6-di-tert-butyl-4-ethylphenol
Conditions | Yield |
---|---|
With copper(l) iodide; 1,8-diazabicyclo[5.4.0]undec-7-ene; 4,4'-di-tert-butyl-2,2'-bipyridine In toluene at 20℃; for 20h; Inert atmosphere; | 80% |
2,6-di-tert-butyl-4-ethylphenol
A
4-Ethylphenol
B
6-di-t-butyl-4-ethylphenol
Conditions | Yield |
---|---|
at 270℃; for 24h; Product distribution; reaction time 8 h; | A 2 % Chromat. B 78% |
at 270℃; for 24h; | A 2 % Chromat. B 78% |
2,6-di-tert-butyl-4-ethylphenol
5,7-di-tert-butyl-2-methyl-1-oxa-spiro[2.5]octa-4,7-dien-6-one
Conditions | Yield |
---|---|
With sodium hypochlorite pentahydrate; tetra-(n-butyl)ammonium iodide In ethyl acetate at 25℃; for 0.5h; Green chemistry; chemoselective reaction; | 77% |
2,6-di-tert-butyl-4-ethylphenol
methoxybenzene
2,6-di-tert-butyl-4-(4-methoxyphenyl)-4-ethylcyclohexa-2,5-dien-1-one
Conditions | Yield |
---|---|
With bis-[(trifluoroacetoxy)iodo]benzene In 1,1,1,3',3',3'-hexafluoro-propanol at 0℃; for 0.0388889h; oxidative Friedel Crafts reaction; regioselective reaction; | 70% |
With bis-[(trifluoroacetoxy)iodo]benzene In 1,1,1,3',3',3'-hexafluoro-propanol oxidative Friedel-Crafts reaction; | 70% |
2,6-di-tert-butyl-4-ethylphenol
sodium benzenesulfonate
2,6-di-tert-butyl-4-(1-(phenylsulfonyl)ethyl)phenol
Conditions | Yield |
---|---|
With tert.-butylhydroperoxide; iodine In chloroform at 20℃; for 12h; regioselective reaction; | 68% |
tert.-butylhydroperoxide
2,6-di-tert-butyl-4-ethylphenol
sodium 4-methylbenzenesulfinate
Conditions | Yield |
---|---|
With iodine In chloroform at 20℃; for 12h; regioselective reaction; | 64% |
Conditions | Yield |
---|---|
With potassium fluoride; sodium azide; silver carbonate In N,N-dimethyl-formamide at 50℃; for 6h; | 63% |
N,N'-(3,3'-bis(propyl)amine)bis(salicylideneiminato)cobalt(II)
2,6-di-tert-butyl-4-ethylphenol
Conditions | Yield |
---|---|
With O2 In dichloromethane mixt. was stirred with O2 bubbling at 0°C for 2-4 h; soln. was concd. in vac. below 20°C, light petroleum was added, soln. was allowed to stand in a refrigerator overnight, crystals were collected, washed with a mixt. of light petroleum and CH2Cl2, dried in vac.; elem. anal.; | 62% |
Conditions | Yield |
---|---|
With potassium fluoride; sodium azide; silver carbonate In N,N-dimethyl-formamide at 50℃; for 6h; | 61% |
tert.-butylhydroperoxide
2,6-di-tert-butyl-4-ethylphenol
sodium 4-fluorobenzenesulfinate
Conditions | Yield |
---|---|
With iodine In chloroform at 20℃; for 12h; regioselective reaction; | 58% |
tert.-butylhydroperoxide
2,6-di-tert-butyl-4-ethylphenol
sodium p-chlorobenzenesulphinate
Conditions | Yield |
---|---|
With iodine In chloroform at 20℃; for 12h; regioselective reaction; | 56% |
2,6-di-tert-butyl-4-ethylphenol
sodium thiophene-2-sulphinate
Conditions | Yield |
---|---|
With tert.-butylhydroperoxide; iodine In chloroform at 20℃; for 12h; regioselective reaction; | 47% |
2,6-di-tert-butyl-4-ethylphenol
2,6-di-tert-butyl-4-(3,5-di-tert-butyl-4-hydroxyphenyl)-4-methyl-2,5-cyclohexadiene-1-one
Conditions | Yield |
---|---|
With 1,8-diazabicyclo[5.4.0]undec-7-ene; copper(ll) bromide In toluene at 20℃; for 1h; Inert atmosphere; | 18% |
2,6-di-tert-butyl-4-ethylphenol
2,6-di-tert-butyl-4-ethylidenecyclohexa-2,5-en-1-one
Conditions | Yield |
---|---|
With potassium hexacyanoferrate(III); benzene | |
With potassium hydroxide; potassium hexacyanoferrate(III) | |
With sodium persulfate; sodium hexacyanoferrate(II) decahydrate; sodium hydroxide In hexane; water for 4h; Inert atmosphere; | |
With sodium peroxydisulfate; sodium hexacyanoferrate(II) decahydrate; sodium hydroxide In hexane; water for 4h; Inert atmosphere; | |
With potassium hydroxide; potassium hexacyanoferrate(III) In water at 23℃; for 1h; Inert atmosphere; |
2,6-di-tert-butyl-4-ethylphenol
1-(3,5-di-tert-butyl-4-hydroxyphenyl)ethanone
Conditions | Yield |
---|---|
With Isopropylbenzene; Cumene hydroperoxide; cobalt(II) o-phthalate at 80 - 100℃; Behandeln mit Luft; |
2,6-di-tert-butyl-4-ethylphenol
A
2-(3,5-di-t-butyl-4-hydroxyphenyl)ethanol
B
1-(3,5-di-tert-butyl-4-hydroxyphenyl)ethanone
Conditions | Yield |
---|---|
With Isopropylbenzene; air; Cumene hydroperoxide; cobalt(II) o-phthalate at 80 - 100℃; |
Molecular Structure:
Molecular Formula: C16H26O
Molecular Weight: 234.377
IUPAC Name: 2,6-Ditert-butyl-4-ethylphenol
Synonyms of Phenol,2,6-bis(1,1-dimethylethyl)-4-ethyl- (CAS NO.4130-42-1): 1-Hydroxy-4-ethyl-2,6-di-tert-butylbenzene ; 2,6-Bis(1,1-dimethylethyl)-4-ethylphenol ; 2,6-Di-tert-butyl-4-ethylphenol ; 4-Ethyl-2,6-di-tert-butylphenol ; CCRIS 8263 ; EINECS 223-945-2 ; Ionol 2 ; NSC 14453 ; Phenol, 2,6-di-tert-butyl-4-ethyl- (8CI) ; Phenol, 2,6-di-tert-butyl-4-ethyl-
CAS NO: 4130-42-1
Classification Code: Aromatic Phenols ; Organics
Melting point: >44°C
Index of Refraction: 1.497
Molar Refractivity: 74.45 cm3
Molar Volume: 254 cm3
Surface Tension: 30 dyne/cm
Density: 0.922 g/cm3
Flash Point: 124.1 °C
Enthalpy of Vaporization: 53.08 kJ/mol
Boiling Point: 272 °C at 760 mmHg
Vapour Pressure: 0.00375 mmHg at 25°C
Risk Statements of Phenol,2,6-bis(1,1-dimethylethyl)-4-ethyl- (CAS NO.4130-42-1): 36/37/38
R36/37/38: Irritating to eyes, respiratory system and skin.
Safety Statements: 26-36
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36: Wear suitable protective clothing.
RIDADR: 3077
HazardClass: 9
PackingGroup: III
About|Contact|Cas|Product Name|Molecular|Country|Encyclopedia
Message|New Cas|MSDS|Service|Advertisement|CAS DataBase|Article Data|Manufacturers | Chemical Catalog
©2008 LookChem.com,License: ICP
NO.:Zhejiang16009103
complaints:service@lookchem.com Desktop View