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CAS No.: | 13879-32-8 |
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Name: | 1,1'-[methylenebis(oxyethane-1,2-diyloxy)]bisbenzene |
Article Data: | 4 |
Molecular Structure: | |
Formula: | C17H20 O4 |
Molecular Weight: | 288.343 |
Synonyms: | Methane,bis(2-phenoxyethoxy)- (6CI,8CI); Bis(phenoxyethoxy)methane; Bis(phenoxyethyl)formal; Bis(b-phenoxyethyl)formal; Desavin |
Density: | 1.106±0.06 g/cm3(Predicted) |
Melting Point: | 18 °C |
Boiling Point: | 195-196 °C(Press: 0.6 Torr) |
Flash Point: | 135.2oC |
PSA: | 36.92000 |
LogP: | 3.13510 |
Conditions | Yield |
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With tetrabutylammomium bromide; potassium hydroxide In benzene for 5h; Reflux; | 59% |
2-Phenoxyethanol
dimethyl sulfoxide
A
bis-[(2-phenoxyethyl)oxy]methane
B
2-chloroethoxybenzene
Conditions | Yield |
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With 2,4-Dichloro-6-methoxy-1,3,5-triazine In toluene at 80℃; for 4h; | A 52% B 35% |
bis(2-chloroethoxy)methane
sodium phenoxide
bis-[(2-phenoxyethyl)oxy]methane
Conditions | Yield |
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at 180℃; |
bis-[(2-phenoxyethyl)oxy]methane
6-(3,5-dimethylbenzyl)-5-ethyl-1,2,3,4-tetrahydropyrimidine-2,4-dione
Conditions | Yield |
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Stage #1: 6-(3,5-dimethylbenzyl)-5-ethyl-1,2,3,4-tetrahydropyrimidine-2,4-dione With N,O-bis-(trimethylsilyl)-acetamide In acetonitrile for 0.166667h; Inert atmosphere; Stage #2: bis-[(2-phenoxyethyl)oxy]methane With trimethylsilyl trifluoromethanesulfonate In acetonitrile at -50 - 20℃; Inert atmosphere; | 63% |
bis-[(2-phenoxyethyl)oxy]methane
6-benzyl-5-isopropylpyrimidine-2,4(1H,3H)-dione
Conditions | Yield |
---|---|
Stage #1: 6-benzyl-5-isopropylpyrimidine-2,4(1H,3H)-dione With N,O-bis-(trimethylsilyl)-acetamide In acetonitrile for 0.166667h; Inert atmosphere; Stage #2: bis-[(2-phenoxyethyl)oxy]methane With trimethylsilyl trifluoromethanesulfonate In acetonitrile at -50 - 20℃; Inert atmosphere; | 59% |
bis-[(2-phenoxyethyl)oxy]methane
6-benzyl-5-ethylpyrimidine-2,4(1H,3H)-dione
Conditions | Yield |
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Stage #1: 6-benzyl-5-ethylpyrimidine-2,4(1H,3H)-dione With N,O-bis-(trimethylsilyl)-acetamide In acetonitrile for 0.166667h; Inert atmosphere; Stage #2: bis-[(2-phenoxyethyl)oxy]methane With trimethylsilyl trifluoromethanesulfonate In acetonitrile at -50 - 20℃; Inert atmosphere; | 48% |
bis-[(2-phenoxyethyl)oxy]methane
6-(3,5-dimethylbenzyl)-5-isopropyl-2,4-pyrimidinedione
Conditions | Yield |
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Stage #1: 6-(3,5-dimethylbenzyl)-5-isopropyl-2,4-pyrimidinedione With N,O-bis-(trimethylsilyl)-acetamide In acetonitrile for 0.166667h; Inert atmosphere; Stage #2: bis-[(2-phenoxyethyl)oxy]methane With trimethylsilyl trifluoromethanesulfonate In acetonitrile at -50 - 20℃; Inert atmosphere; |
bis-[(2-phenoxyethyl)oxy]methane
Conditions | Yield |
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Stage #1: 5-ethyl-6-(3,5-dimethoxybenzyl)uracil With N,O-bis-(trimethylsilyl)-acetamide In acetonitrile for 0.166667h; Inert atmosphere; Stage #2: bis-[(2-phenoxyethyl)oxy]methane With trimethylsilyl trifluoromethanesulfonate In acetonitrile at -50 - 20℃; Inert atmosphere; |
bis-[(2-phenoxyethyl)oxy]methane
Conditions | Yield |
---|---|
Stage #1: 5-isopropyl-6-(3,5-dimethoxybenzyl)uracil With N,O-bis-(trimethylsilyl)-acetamide In acetonitrile for 0.166667h; Inert atmosphere; Stage #2: bis-[(2-phenoxyethyl)oxy]methane With trimethylsilyl trifluoromethanesulfonate In acetonitrile at -50 - 20℃; Inert atmosphere; |