Conditions | Yield |
---|---|
With N-Bromosuccinimide; L-proline In water at 20℃; for 1h; | 95% |
With Oxone; sodium chloride In water; ethyl acetate at 20℃; for 3.5h; | 90% |
With air; [IrCl(coe)2]2 at 95℃; for 15h; | 68% |
Conditions | Yield |
---|---|
With bis(1,5-cyclooctadiene)nickel(0); 1,3-bis-(2,6-diisopropylphenyl)-4,5-dichloroimidazol-2-ylidene In toluene at 23 - 60℃; Tishchenko reaction; Inert atmosphere; | 94% |
With trimethylaluminum; benzene-1,2-diol; isopropyl alcohol In dichloromethane at 20℃; for 2h; | 86% |
With magnesium aluminium-alcoholate | |
With aluminum isopropoxide |
2-Ethylhexyl alcohol
A
2-ethylhexyl 2-ethylhexanoate
B
2-ethylhexanoyl fluoride
Conditions | Yield |
---|---|
With bromine trifluoride In chloroform; trichlorofluoromethane | A 10% B 85% |
d,l-2-ethylhexanal
A
2-Ethylhexyl alcohol
B
2-ethylhexyl 2-ethylhexanoate
Conditions | Yield |
---|---|
With methanol; [carbonylchlorohydrido{bis[2-(diphenylphosphinomethyl)ethyl]amino}ethylamino] ruthenium(II); sodium methylate at 90℃; for 6h; | A 13.9% B 15.3% |
With [carbonylchlorohydrido{bis[2-(diphenylphosphinomethyl)ethyl]amino}ethylamino] ruthenium(II); sodium methylate In methanol at 90℃; for 6h; Reagent/catalyst; | A 15.3% B 13.9% |
With methanol; [2-(di-tert-butylphosphinomethyl)-6-(diethylaminomethyl)pyridine]ruthenium(II) chlorocarbonyl hydride; sodium methylate at 90℃; for 6h; | A 13.2% B 11.6% |
2-Ethylhexyl alcohol
A
2-Ethylhexanoic acid
B
2-ethylhexyl 2-ethylhexanoate
Conditions | Yield |
---|---|
With pyridine; 1,2-Dichloro-3-iodobenzene for 24h; Mechanism; Ambient temperature; method for oxidation of saturated alcohols to acid chlorides (acids) and esters; | A 66.88 % Chromat. B 15.49 % Chromat. |
With pyridine; 1,2-Dichloro-3-iodobenzene for 24h; Ambient temperature; Title compound not separated from byproducts; | A 66.88 % Chromat. B 15.42 % Chromat. |
Conditions | Yield |
---|---|
With 2-Ethylhexyl alcohol at 50℃; |
d,l-2-ethylhexanal
A
2-Ethylhexyl alcohol
B
2-Ethylhexanoic acid
C
2-ethylhexyl 2-ethylhexanoate
Conditions | Yield |
---|---|
in verschiedenen Loesungsmitteln; |
2-Ethylhexyl alcohol
A
d,l-2-ethylhexanal
B
2-Ethylhexanoic acid
C
2-ethylhexyl 2-ethylhexanoate
Conditions | Yield |
---|---|
With potassium dichromate; sulfuric acid; acetic acid In water; Petroleum ether at 25℃; Reagent/catalyst; |
2-Ethylhexyl alcohol
toluene
A
2-ethylhexyl 2-ethylhexanoate
B
Velate 368
Conditions | Yield |
---|---|
With Oxone; Pyridine-2,6-dicarboxylic acid; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; tetrabutylammomium bromide; iron(II) acetate at 110℃; for 48h; Sealed tube; | A 70 %Chromat. B n/a |
2-Ethylhexyl alcohol
A
d,l-2-ethylhexanal
B
2-Ethylhexanoic acid
C
2-ethylhexyl 2-ethylhexanoate
D
2-ethylhexanol nitrate
Conditions | Yield |
---|---|
With nitric acid; urea; cerium triflate In 1,2-dichloro-ethane at 90℃; for 5h; Reagent/catalyst; |
1. | skn-rbt 10 mg/24H open MLD | AIHAAP American Industrial Hygiene Association Journal. 23 (1962),95. | ||
2. | eye-rbt 500 mg | AJOPAA American Journal of Ophthalmology. 29 (1946),1363. | ||
3. | orl-rat LD50:27 g/kg | AIHAAP American Industrial Hygiene Association Journal. 23 (1962),95. |
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