Conditions | Yield |
---|---|
With copper(l) chloride; potassium hydroxide at 20℃; for 8h; Neat (no solvent); | 99% |
With aluminum oxide; copper; potassium hydroxide for 0.5h; | 98% |
With copper(l) iodide; bis(tetrabutylammonium) adipate; L-proline In N,N-dimethyl-formamide at 25℃; for 24h; Inert atmosphere; | 96% |
Conditions | Yield |
---|---|
With copper(l) chloride; potassium hydroxide at 90℃; for 8h; Neat (no solvent); | 99% |
With potassium phosphate; copper(l) iodide In diethylene glycol at 70℃; for 14h; Sealed tube; | 98% |
With copper(l) iodide; potassium carbonate In water at 80℃; for 15h; | 91.1% |
With chitosan Cu2+ complex In acetonitrile for 6h; Reflux; Green chemistry; | 87% |
Conditions | Yield |
---|---|
With [copper(II)]2-β-cyclodextrin complex In water at 20℃; for 24h; chemoselective reaction; | 96% |
With Fe3O4 magnetic nanoparticles-supported EDTA-copper(II) complex In water at 50℃; for 2h; Green chemistry; | 96% |
Conditions | Yield |
---|---|
With Na-Y zeolite In Triethylene glycol dimethyl ether at 160℃; for 0.5h; | 94% |
With 1-n-butyl-3-methylimidazolim bromide |
Conditions | Yield |
---|---|
With samarium(III) chloride In tetrahydrofuran at 0℃; for 12h; | 93.1% |
With zinc(II) chloride In acetonitrile at -20℃; for 20h; | 87.3% |
In acetone for 15h; Cooling with ice; | 82% |
Conditions | Yield |
---|---|
at 90℃; for 6h; Inert atmosphere; | 90% |
Conditions | Yield |
---|---|
at 90℃; for 4h; Inert atmosphere; | 89% |
at 80℃; for 1h; | 3 g |
thiophenol
A
diphenyl sulfide
B
diphenyldisulfane
C
Azobenzene
D
2-Anilinoethanol
Conditions | Yield |
---|---|
In phosphate buffer; acetonitrile at 25℃; for 4h; pH=7.4; Oxidation; Ring cleavage; Further byproducts given; | A 3% B 85% C 7.5% D 1.7% |
Conditions | Yield |
---|---|
With 3,6‐di‐tert‐butyl‐9‐mesityl‐10‐phenylacridin‐10‐ium tetrafluoroborate In 2,2,2-trifluoroethanol at 29℃; for 24h; Reagent/catalyst; Solvent; Sealed tube; Irradiation; Inert atmosphere; | 85% |
Conditions | Yield |
---|---|
With Fe3O4/FeO In water at 40℃; for 24h; Time; Green chemistry; | 76% |
With palladium on activated charcoal; zinc(II) oxide In water at 150℃; for 24h; Sealed tube; | 65% |
In o-xylene at 150℃; for 30h; Inert atmosphere; Sealed tube; | 39% |
tiveTMNano*MgO*Plus*(NAP-MgO,*Aerogel*prepared) at 125℃; for 1h; |
[1,3]-dioxolan-2-one
aniline
A
2,2'-(phenylimino)bis[ethanol]
B
2-Anilinoethanol
Conditions | Yield |
---|---|
With tri-i-butyl(methyl)phosphonium tosylate at 170℃; for 8h; Ionic liquid; Neat (no solvent); | A 74% B n/a |
With Na-Y zeolite In Triethylene glycol dimethyl ether at 160℃; for 2h; | A 19% B 63% |
In neat (no solvent) at 140℃; for 14h; |
Conditions | Yield |
---|---|
Stage #1: Glycolaldehyde; aniline In 1,2-dichloro-ethane at 20℃; for 0.5h; Inert atmosphere; Stage #2: With sodium tris(acetoxy)borohydride In 1,2-dichloro-ethane for 4h; | 72% |
Conditions | Yield |
---|---|
With potassium phosphate; copper diacetate In 1,4-dioxane at 40℃; for 24h; Inert atmosphere; | 60% |
triphenylbismuth(V) diacetate
ethanolamine
A
N,N-diphenyl-N-(2-hydroxyethyl)amine
B
N-(2-phenoxyethyl)aniline
C
2-Anilinoethanol
Conditions | Yield |
---|---|
A 8% B 17% C 51% |
Conditions | Yield |
---|---|
With copper In N,N-dimethyl-formamide Reflux; | 46% |
Conditions | Yield |
---|---|
With potassium carbonate; potassium iodide at 80℃; for 12h; Inert atmosphere; | 41% |
at 110℃; |
3-phenylcyclohexanospiro-2-oxazolidine
A
1-phenyl-4,5,6,7-tetrahydro-1H-indole
B
2-Anilinoethanol
C
cyclohexanol
Conditions | Yield |
---|---|
With potassium hydroxide Heating; CH3ONa as reagent; | A 38% B n/a C n/a |
methanol
formaldehyd
aniline
A
2,2'-(phenylimino)bis[ethanol]
B
2-Anilinoethanol
Conditions | Yield |
---|---|
With tert.-butylhydroperoxide; titanium(III) chloride at 20℃; for 0.5h; Acidic aq. solution; Inert atmosphere; | A 15% B 30% |
Conditions | Yield |
---|---|
With [Ir(κ2O,O-CH3COO)(I)2{κC,C'-methylenebis(N-methyl)imidazole-2-ylidene}]; water; glycerol; potassium hydroxide at 120℃; for 16h; | 22% |
N-methyl-2-phenoxyethan-1-amine
A
N-(2-hydroxyethyl)-N-methylaminobenzene
B
2-Anilinoethanol
Conditions | Yield |
---|---|
With 3,6‐di‐tert‐butyl‐9‐mesityl‐10‐phenylacridin‐10‐ium tetrafluoroborate In 2,2,2-trifluoroethanol at 29℃; for 24h; Sealed tube; Irradiation; Inert atmosphere; | A 15% B 8% |
Conditions | Yield |
---|---|
With ethanol; sodium |
Conditions | Yield |
---|---|
With alkaline solution; water | |
With ethanol; alkaline solution |
4-((2-hydroxyethyl)amino)benzoic acid
2-Anilinoethanol
Conditions | Yield |
---|---|
at 210 - 260℃; |
4-((2-hydroxyethyl)amino)benzoic acid
A
methylammonium carbonate
B
2-Anilinoethanol
Conditions | Yield |
---|---|
at 210 - 260℃; |
ethylene glycol
aniline
A
2,2'-(phenylimino)bis[ethanol]
B
2-Anilinoethanol
Conditions | Yield |
---|---|
With boron trifluoride at 190℃; |
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride |
aniline
2-chloro-ethanol
A
1,4-diphenyl-piperazine
B
2,2'-(phenylimino)bis[ethanol]
C
N,N'-diphenylethylenediamine
D
2-Anilinoethanol
Conditions | Yield |
---|---|
at 110℃; | |
at 110℃; |
aniline
2-chloro-ethanol
A
1,4-diphenyl-piperazine
B
2,2'-(phenylimino)bis[ethanol]
C
2-Anilinoethanol
Conditions | Yield |
---|---|
at 110℃; |
aniline
2-chloro-ethanol
A
N,N'-diphenylethylenediamine
B
2-Anilinoethanol
Conditions | Yield |
---|---|
at 180℃; |
aniline
2-chloro-ethanol
A
2,2'-(phenylimino)bis[ethanol]
B
2-Anilinoethanol
Conditions | Yield |
---|---|
With water; calcium carbonate | |
With sodium carbonate | |
With 1-butyl-3-methylimidazolium Tetrafluoroborate at 100℃; for 6h; Time; Temperature; Concentration; |
The 2-Anilinoethanol, with the CAS registry number 122-98-5, is also known as N-(2-Hydroxyethyl)aniline. It belongs to the product categories of Intermediates of Dyes and Pigments; Hydroxyethylamines. Its EINECS registry number is 204-588-1. This chemical's molecular formula is C8H11NO and molecular weight is 137.18. What's more, its IUPAC name is the same with its product name.
Physical properties about 2-Anilinoethanol are: (1)ACD/LogP: 0.906; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 0.86; (4)ACD/LogD (pH 7.4): 0.91; (5)ACD/BCF (pH 5.5): 2.60; (6)ACD/BCF (pH 7.4): 2.87; (7)ACD/KOC (pH 5.5): 66.98; (8)ACD/KOC (pH 7.4): 73.97; (9)#H bond acceptors: 2; (10)#H bond donors: 2; (11)#Freely Rotating Bonds: 4; (12)Polar Surface Area: 32.26 Å2; (13)Index of Refraction: 1.6; (14)Molar Refractivity: 42.03 cm3; (15)Molar Volume: 122.902 cm3; (16)Polarizability: 16.662×10-24cm3; (17)Surface Tension: 47.517 dyne/cm; (18)Density: 1.116 g/cm3; (19)Flash Point: 151.359 °C; (20)Enthalpy of Vaporization: 55.556 kJ/mol; (21)Boiling Point: 286.882 °C at 760 mmHg; (22)Vapour Pressure: 0.001 mmHg at 25 °C.
Preparation of 2-Anilinoethanol: this chemical can be prepared by benzenethiol with 3-phenyl-4,5-dihydro-[1,2,3]oxadiazol-3-ium; trifluoro-methanesulfonate. This reaction type is Oxidation//Ring cleavage. This reaction needs solvents acetonitrile and phosphate buffer at temperature of 25 °C. The reaction time is 4 hours and the value of PH is 7.4. The yield is 85 %.
Uses of 2-Anilinoethanol: it is used to produce other chemicals. For example, it can react with 1-fluoro-2-nitro-benzene to get N-[2-(2-nitrophenoxy)ethyl]aniline. This reaction needs reagent KOH and solvents benzene at temperature of 100 °C. The reaction time is 20 hours. The yield is 85 %.
When you are dealing with this chemical, you should be very careful. This chemical cause damage to health at low levels and it is toxic in contact with skin. It is harmful by inhalation, in contact with skin and if swallowed. In addition, it is irritating to eyes and it is has serious damage to eyes. Therefore, you should wear suitable protective clothing, gloves and eye/face protection. In case of contacting with eyes, you should rinse immediately with plenty of water and seek medical advice. And in case of accident or if you feel unwell seek medical advice immediately.
You can still convert the following datas into molecular structure:
(1) SMILES: OCCNc1ccccc1
(2) InChI: InChI=1S/C8H11NO/c10-7-6-9-8-4-2-1-3-5-8/h1-5,9-10H,6-7H2
(3) InChIKey: MWGATWIBSKHFMR-UHFFFAOYSA-N
The toxicity data is as follows:
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
dog | LDLo | intravenous | 165mg/kg (165mg/kg) | VASCULAR: CONTRACTION (ISOLATED TISSUES) | JAMA, Journal of the American Medical Association. Vol. 123, Pg. 761, 1943. |
dog | LDLo | subcutaneous | 220mg/kg (220mg/kg) | VASCULAR: CONTRACTION (ISOLATED TISSUES) | JAMA, Journal of the American Medical Association. Vol. 123, Pg. 761, 1943. |
mouse | LD50 | intraperitoneal | 137mg/kg (137mg/kg) | Yakugaku Zasshi. Journal of Pharmacy. Vol. 97, Pg. 1117, 1977. | |
mouse | LDLo | subcutaneous | 1100mg/kg (1100mg/kg) | VASCULAR: BP ELEVATION NOT CHARACTERIZED IN AUTONOMIC SECTION | "Structure et Activite Pharmacodyanmique des Medicaments du Systeme Nerveux Vegetatif," Bovet, D., and F. Bovet-Nitti, New York, S. Karger, 1948Vol. -, Pg. 111, 1948. |
rabbit | LD50 | skin | 63uL/kg (.063mL/kg) | American Industrial Hygiene Association Journal. Vol. 23, Pg. 95, 1962. | |
rabbit | LDLo | intravenous | 44mg/kg (44mg/kg) | BEHAVIORAL: COMA BEHAVIORAL: ATAXIA | JAMA, Journal of the American Medical Association. Vol. 123, Pg. 761, 1943. |
rat | LD50 | oral | 2230mg/kg (2230mg/kg) | Union Carbide Data Sheet. Vol. 8/21/1961, |
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