3-(benzyloxy)oxetane
oxetan-3-ol
Conditions | Yield |
---|---|
With palladium 10% on activated carbon; hydrogen In methanol at 40℃; under 7600.51 Torr; for 24h; Autoclave; | 95.84% |
3-(1-Ethoxyethoxy)oxetane
oxetan-3-ol
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In methanol at 15 - 18℃; for 0.75h; | 95% |
With toluene-4-sulfonic acid In methanol at 0 - 20℃; for 1h; Reagent/catalyst; Solvent; Large scale; | 79.2% |
With toluene-4-sulfonic acid In methanol at 20℃; for 1h; Reagent/catalyst; Large scale; | 79% |
3-tetrahydropyranyloxyoxetane
oxetan-3-ol
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In methanol deprotection; |
3-chloro-2-hydroxy-1-propyl acetate
ethyl vinyl ether
epichlorohydrin
oxetan-3-ol
Conditions | Yield |
---|---|
With sodium hydroxide; iron(III) chloride; toluene-4-sulfonic acid In water; acetic acid |
Conditions | Yield |
---|---|
With sodium tetrahydroborate In tetrahydrofuran at 25℃; for 4h; | 1 g |
With sodium tetrahydroborate In tetrahydrofuran at 25℃; for 4h; | 1 g |
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0 - 20℃; for 3h; | 100% |
Stage #1: oxetan-3-ol With triethylamine In dichloromethane at 0℃; for 0.333333h; Stage #2: methanesulfonyl chloride In dichloromethane at 20℃; for 12h; | 75.7% |
With triethylamine In dichloromethane at 20℃; for 5.5h; Cooling with ice; Inert atmosphere; | 68% |
oxetan-3-ol
p-toluenesulfonyl chloride
oxetan-3-yl 4-methylbenzenesulfonate
Conditions | Yield |
---|---|
With dmap; triethylamine In dichloromethane at 20℃; for 2h; | 95% |
With triethylamine In water at 20℃; for 18h; | 94% |
With sodium hydroxide In water ice-bath cooling; | 93% |
Conditions | Yield |
---|---|
With sodium hydroxide In water | 94% |
Conditions | Yield |
---|---|
With cesium fluoride In acetonitrile at 100℃; for 15h; Sealed tube; | 94% |
Conditions | Yield |
---|---|
With N1,N2-bis(naphthalen-1-ylmethyl)oxalamide; potassium tert-butylate; copper diacetate In 1,4-dioxane at 100℃; for 24h; Schlenk technique; Inert atmosphere; Molecular sieve; | 94% |
Conditions | Yield |
---|---|
Stage #1: oxetan-3-ol With sodium hydride In N,N-dimethyl-formamide; mineral oil at 0℃; for 0.5h; Stage #2: 5-fluoropicolinonitrile In N,N-dimethyl-formamide; mineral oil at 0℃; for 0.5h; | 92.41% |
Conditions | Yield |
---|---|
Stage #1: oxetan-3-ol With sodium hydride In N,N-dimethyl-formamide; mineral oil at 0℃; for 1h; Stage #2: 3-chloro-2-fluoro-4-iodopyridine In N,N-dimethyl-formamide; mineral oil at 20℃; for 1h; | 91% |
With caesium carbonate In dimethyl sulfoxide at 100℃; for 1.5h; | 37% |
oxetan-3-ol
2-fluoro-5-nitrobenzonitrile
Conditions | Yield |
---|---|
Stage #1: oxetan-3-ol With potassium tert-butylate In tetrahydrofuran at 0℃; for 0.333333h; Inert atmosphere; Stage #2: 2-fluoro-5-nitrobenzonitrile In tetrahydrofuran at 0 - 20℃; for 1.16667h; | 90% |
oxetan-3-ol
Conditions | Yield |
---|---|
With sodium hydride In tetrahydrofuran at 20℃; for 2h; Inert atmosphere; | 88% |
Stage #1: oxetan-3-ol With sodium hydride In tetrahydrofuran Inert atmosphere; Stage #2: ethyl 6-chloro-2-(3-iodophenyl)pyrimidine-4-carboxylate In tetrahydrofuran at 20℃; for 2h; Inert atmosphere; |
Conditions | Yield |
---|---|
With di-isopropyl azodicarboxylate; triphenylphosphine In tetrahydrofuran at 20℃; for 18h; | 87% |
Conditions | Yield |
---|---|
With di-isopropyl azodicarboxylate; triphenylphosphine In tetrahydrofuran at 20℃; for 18h; | 86% |
With di-isopropyl azodicarboxylate; triphenylphosphine In tetrahydrofuran at 20℃; for 18h; | 86% |
oxetan-3-ol
2-chloro-N-[(3-fluorophenyl)-methyl]-4-methyl-6-morpholin-4-yl-pyridine-3-carboxylic acid amide
N-[(3-fluorophenyl)-methyl]-4-methyl-6-morpholin-4-yl-2-(oxetan-3-yloxy)-pyridine-3-carboxylic acid amide
Conditions | Yield |
---|---|
Stage #1: oxetan-3-ol With potassium tert-butylate In tetrahydrofuran at 50℃; for 0.25h; Stage #2: 2-chloro-N-[(3-fluorophenyl)-methyl]-4-methyl-6-morpholin-4-yl-pyridine-3-carboxylic acid amide In tetrahydrofuran at 80℃; for 8h; | 84% |
oxetan-3-ol
6-chloro-N-[(3-fluorophenyl)-methyl]-4-methyl-2-morpholin-4-yl-pyridine-3-carboxylic acid amide
N-[(3-fluorophenyl)-methyl]-4-methyl-6-morpholin-4-yl-2-(oxetan-3-yloxy)-pyridine-3-carboxylic acid amide
Conditions | Yield |
---|---|
Stage #1: oxetan-3-ol With potassium tert-butylate at 50℃; for 0.25h; Stage #2: 6-chloro-N-[(3-fluorophenyl)-methyl]-4-methyl-2-morpholin-4-yl-pyridine-3-carboxylic acid amide In tetrahydrofuran at 80℃; for 8h; | 84% |
Conditions | Yield |
---|---|
Stage #1: oxetan-3-ol With sodium hydride In tetrahydrofuran at 0 - 20℃; for 0.5h; Stage #2: benzyl bromide In tetrahydrofuran at 60℃; | 84% |
Stage #1: oxetan-3-ol With sodium hydride In tetrahydrofuran at 0℃; for 0.5h; Inert atmosphere; Stage #2: benzyl bromide In tetrahydrofuran at 0 - 20℃; Inert atmosphere; | 63% |
Conditions | Yield |
---|---|
With caesium carbonate In dimethyl sulfoxide at 23℃; for 12h; Schlenk technique; | 84% |
Conditions | Yield |
---|---|
Stage #1: oxetan-3-ol With sodium hydride In N,N-dimethyl-formamide; mineral oil at 0℃; for 0.5h; Inert atmosphere; Stage #2: 2,6-dichloropyridine-4-carboxylic acid In N,N-dimethyl-formamide; mineral oil at 50℃; | 83% |
Conditions | Yield |
---|---|
Stage #1: oxetan-3-ol With sodium hydride In tetrahydrofuran; mineral oil at 0 - 20℃; for 2h; Inert atmosphere; Stage #2: ethyl bromoacetate In tetrahydrofuran; mineral oil at 0 - 20℃; for 12h; Inert atmosphere; | 82% |
Stage #1: oxetan-3-ol With sodium hydride In tetrahydrofuran at 0℃; for 0.5h; Inert atmosphere; Stage #2: ethyl bromoacetate In tetrahydrofuran at 0 - 20℃; for 2h; Inert atmosphere; | 59% |
Conditions | Yield |
---|---|
With di-isopropyl azodicarboxylate; triphenylphosphine In tetrahydrofuran at 20℃; for 18h; | 82% |
With di-isopropyl azodicarboxylate; triphenylphosphine In tetrahydrofuran at 20℃; for 18h; | 82% |
Conditions | Yield |
---|---|
Stage #1: oxetan-3-ol With sodium hydride In tetrahydrofuran at 20℃; for 0.166667h; Stage #2: 4-chloro-3-nitropyridine In tetrahydrofuran at 20℃; for 1h; | 81% |
Stage #1: oxetan-3-ol With sodium hydride In tetrahydrofuran at 20℃; for 0.166667h; Stage #2: 4-chloro-3-nitropyridine In tetrahydrofuran at 20℃; for 1h; | 81% |
Stage #1: oxetan-3-ol With sodium hydride In tetrahydrofuran at 20℃; for 0.166667h; Stage #2: 4-chloro-3-nitropyridine In tetrahydrofuran at 20℃; for 1h; | 81% |
Stage #1: oxetan-3-ol With sodium hydride In tetrahydrofuran at 20℃; for 0.166667h; Stage #2: 4-chloro-3-nitropyridine In tetrahydrofuran at 20℃; for 1h; | 81% |
Conditions | Yield |
---|---|
With di-tert-butyl-diazodicarboxylate; triphenylphosphine In tetrahydrofuran at 20℃; | 80% |
With di-tert-butyl-diazodicarboxylate; triphenylphosphine In tetrahydrofuran at 0 - 20℃; for 16h; | 74% |
Conditions | Yield |
---|---|
With cesium fluoride In acetonitrile at 100℃; for 15h; Sealed tube; | 80% |
oxetan-3-ol
tert-butyldimethylsilyl chloride
Conditions | Yield |
---|---|
With 1H-imidazole In N,N-dimethyl-formamide at 20℃; | 79% |
oxetan-3-ol
Conditions | Yield |
---|---|
With tris-(dibenzylideneacetone)dipalladium(0); caesium carbonate; tert-butyl XPhos In toluene at 90℃; Inert atmosphere; | 79% |
oxetan-3-ol
Conditions | Yield |
---|---|
With lithium tetrafluoroborate; 12-phenyl-12H-benzo[b]phenothiazine In acetonitrile at 0.4℃; for 24h; Irradiation; Inert atmosphere; | 79% |
oxetan-3-ol
tert-butyl benzoyl(tert-butoxycarbonyl)carbamate
Conditions | Yield |
---|---|
With cesium fluoride In acetonitrile at 100℃; for 15h; Sealed tube; | 77% |
oxetan-3-ol
bis(trichloromethyl) carbonate
ethyl 2-(3-Amino-5-bromopyridin-2-yl)acetate
Conditions | Yield |
---|---|
Stage #1: bis(trichloromethyl) carbonate With pyridine In dichloromethane at 0℃; for 0.166667h; Stage #2: oxetan-3-ol In dichloromethane for 1h; Stage #3: ethyl 2-(3-Amino-5-bromopyridin-2-yl)acetate With pyridine In dichloromethane at 20℃; | 75% |
Empirical Formula: C3H6O2
Molecular Weight: 74.0785
Nominal Mass: 74 Da
Average Mass: 74.0785 Da
Monoisotopic Mass: 74.036779 Da
Index of Refraction: 1.489
Molar Refractivity: 17.031 cm3
Molar Volume: 59.008 cm3
Surface Tension: 43.414 dyne/cm
Density: 1.255 g/cm3
Flash Point: 77.266 °C
Enthalpy of Vaporization: 45.417 kJ/mol
Boiling Point: 153.124 °C at 760 mmHg
Vapour Pressure: 1.255 mmHg at 25 °C
Structure of Oxetan-3-Ol (CAS NO.7748-36-9):
Product Category of Oxetan-3-Ol (CAS NO.7748-36-9): Alcohols and Derivatives;Heterocycles;API intermediates
Oxetan-3-Ol , its cas register number is 7748-36-9. It also can be called 2-Propanol,1,3-epoxy- (7CI,8CI) ; 3-Oxetanol ; and 3-Hydroxyoxetane .
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