polytetrafluoroethylene
4-hexafluoroisopropylidene-1,3,2-dioxathietane 2,2-dioxide
A
tetrafluoroethane-β-sultone
B
bis(trifluoromethyl)ketene
Conditions | Yield |
---|---|
40-50°C; | A 96% B n/a |
40-50°C; | A 96% B n/a |
Conditions | Yield |
---|---|
fresh distilled SO3, 2.7 atm, below 80°C, 1 h; | 93% |
fresh distilled SO3, 2.7 atm, below 80°C, 1 h; | 93% |
fresh distilled SO3, 2.7 atm, below 80°C, 1 h; | 93% |
Conditions | Yield |
---|---|
With sulfur trioxide for 2h; Cycloaddition; | 82% |
With sulfur trioxide | |
With sulfur trioxide |
polytetrafluoroethylene
sulfur trioxide
A
tetrafluoroethane-β-sultone
B
5,5,6,6-tetrafluoro-2,2,4,4-tetroxo-1,3-dioxa-2,4-dithiane
polytetrafluoroethylene
1,1,2-Trichloro-1,2,2-trifluoroethane
sulfur trioxide
tetrafluoroethane-β-sultone
Conditions | Yield |
---|---|
with C2F4 satd. CFCl2CF2Cl adn. to SO3 under 2.4 h,standing for a night at room temp.; | |
with C2F4 satd. CFCl2CF2Cl adn. to SO3 under 2.4 h,standing for a night at room temp.; |
polytetrafluoroethylene
A
tetrafluoroethane-β-sultone
B
4,4,5,5-Tetrafluor-2-oxo-1,3,2-dioxathiolan
Conditions | Yield |
---|---|
With O3S at 20 - 50℃; under 767.652 - 3040.2 Torr; for 6h; Large scale; |
Conditions | Yield |
---|---|
With water | 100% |
With water | 78% |
With water | |
With water | |
With water |
tetrafluoroethane-β-sultone
potassium tetrafluoro(2-fluorosulfonyl)-1-ethanolate
Conditions | Yield |
---|---|
With potassium fluoride In diethylene glycol dimethyl ether | 100% |
With potassium fluoride; diethylene glycol dimethyl ether Cooling with ice; |
Conditions | Yield |
---|---|
for 0.5h; Autoclave; Cooling with ice; | 100% |
In diethylene glycol dimethyl ether Cooling with ice; |
tetrafluoroethane-β-sultone
aniline
1,1-difluoro-2-oxo-(phenylamino)ethanesulfonic acid fluoride
Conditions | Yield |
---|---|
In diethyl ether at -80°C; | 98% |
In diethyl ether at -80°C; | 98% |
tetrafluoroethane-β-sultone
nitrosylchloride
chlorosulfuric acid trifluorovinyl ester
Conditions | Yield |
---|---|
at -35°C; | 97% |
at -35°C; | 97% |
Conditions | Yield |
---|---|
In petroleum ether at 25°C; | 96% |
In Petroleum ether at 25°C; | 96% |
In Petroleum ether |
tetrafluoroethane-β-sultone
water
2,2-difluoro-2-(fluorosulfonyl)acetic acid
Conditions | Yield |
---|---|
In neat (no solvent) at 5°C, with polytetrafluoroethylene filled reactor used; distn.; | 96% |
In Petroleum ether at -10°C; | 62% |
In petroleum ether at -10°C; | 62% |
methanol
tetrafluoroethane-β-sultone
2,2-difluoro-2-(fluorosulfonyl)acetate
Conditions | Yield |
---|---|
at 0-5°C; | 95% |
tetrafluoroethane-β-sultone
ethanol
ethyl 2,2-difluoro-2-(fluorosulfonyl)acetate
Conditions | Yield |
---|---|
at 0-5°C; | 95% |
tetrafluoroethane-β-sultone
methanesulfonyl chloride
A
methyl fluorosulfonate
B
chlorosulfuric acid trifluorovinyl ester
Conditions | Yield |
---|---|
at room temp.; | A 90% B 95% |
at room temp.; | A 90% B 95% |
methylphosphonic acid dichloroanhydride
tetrafluoroethane-β-sultone
chlorosulfuric acid trifluorovinyl ester
Conditions | Yield |
---|---|
In dichloromethane at -10°C; | 94% |
In dichloromethane at -10°C; | 94% |
tetrafluoroethane-β-sultone
isopropyl alcohol
difluoro-fluorosulfonyl-acetic acid isopropyl ester
Conditions | Yield |
---|---|
at 0-5°C; | 93% |
In diethyl ether at 10°C; | 30% |
tetrafluoroethane-β-sultone
trichlorophosphate
chlorosulfuric acid trifluorovinyl ester
Conditions | Yield |
---|---|
at 20°C; | 91% |
at 20°C; | 91% |
tetrafluoroethane-β-sultone
2,2,2-trifluoroethanol
Difluoro-fluorosulfonyl-acetic acid 2,2,2-trifluoro-ethyl ester
Conditions | Yield |
---|---|
With sodium fluoride at 25℃; for 24h; other sulton, various alcohols; | 90% |
tetrafluoroethane-β-sultone
2,2,3,3-tetrafluoropropanol
Difluor(fluorsulfonyl-)essigsaeure-1,1,2,2-tetrafluorpropylester
Conditions | Yield |
---|---|
With sodium fluoride at 25℃; for 24h; | 90% |
Conditions | Yield |
---|---|
With sulfuric acid at 20°C, 100 % H2SO4 used; | 90% |
With H2SO4 at 20°C, 100 % H2SO4 used; | 90% |
tetrafluoroethane-β-sultone
sodium methylate
Methoxysulfonyl-difluor-essigsaeure-methylester
Conditions | Yield |
---|---|
In diethyl ether in mixture of ice-NaCl; | 86% |
In diethyl ether in mixture of ice-NaCl; | 86% |
In methanol |
Conditions | Yield |
---|---|
at 0-5°C; | 86% |
With sodium fluoride for 7h; Ambient temperature; | 76.6% |
tetrafluoroethane-β-sultone
sodium ethanolate
Ethoxysulfonyl-difluor-essigsaeure-ethylester
Conditions | Yield |
---|---|
In diethyl ether in mixture of ice-NaCl; | 85% |
In diethyl ether in mixture of ice-NaCl; | 85% |
In ethanol |
Hexafluoropropene oxide
tetrafluoroethane-β-sultone
perfluoro(4-methyl-3,6-dioxaoct-7-ene)sulfonyl fluoride
Conditions | Yield |
---|---|
Stage #1: Hexafluoropropene oxide; tetrafluoroethane-β-sultone With potassium fluoride In N,N-dimethyl acetamide at 20℃; under 3000.3 Torr; for 1h; Stage #2: With potassium carbonate at 150 - 360℃; for 0.583333h; Pressure; Temperature; Solvent; Reagent/catalyst; | 85% |
tetrafluoroethane-β-sultone
aniline
difluoro-phenylcarbamoyl-methanesulfonic acid ; compound with aniline
Conditions | Yield |
---|---|
In diethyl ether at 10°C; | 84% |
In diethyl ether at 10°C; | 84% |
Conditions | Yield |
---|---|
at 0°C; | 82% |
Conditions | Yield |
---|---|
at -20°C; | 82% |
tetrafluoroethane-β-sultone
chlorosulfuric acid pentyl ester
A
fluorosulfuric acid pentyl ester
B
chlorosulfuric acid trifluorovinyl ester
Conditions | Yield |
---|---|
warming on water bath under reflux, at 30-40°C, 1 h; | A 68% B 80% |
warming on water bath under reflux, at 30-40°C, 1 h; | A 68% B 80% |
tetrafluoroethane-β-sultone
sulfurous acid dibutyl ester
B
1-butyl fluorosulfate
C
sulfuric acid butyl ester trifluorovinyl ester
Conditions | Yield |
---|---|
at -20°C; the products can not separeted by distn.; | A n/a B n/a C 80% |
tetrafluoroethane-β-sultone
chlorosulfuric acid hexyl ester
A
n-hexyl fluorosulfonate
B
chlorosulfuric acid trifluorovinyl ester
Conditions | Yield |
---|---|
warming on water bath under reflux, at 30-40°C, 1 h; | A 76% B 80% |
warming on water bath under reflux, at 30-40°C, 1 h; | A 76% B 80% |
tetrafluoroethane-β-sultone
sulfuric acid dibutyl ester
B
1-butyl fluorosulfate
C
sulfuric acid butyl ester trifluorovinyl ester
Conditions | Yield |
---|---|
at 0°C; | A n/a B n/a C 80% |
Molecular Structure of Tetrafluoroethane beta-sultone (CAS No.697-18-7):
Molecular Formula: C2F4O3S
Molecular Weight: 180.0782
CAS No: 697-18-7
H bond acceptors: 3
H bond donors: 0
Freely Rotating Bonds: 0
Polar Surface Area: 51.75 Å2
Index of Refraction: 1.362
Molar Refractivity: 20.3 cm3
Molar Volume: 91.5 cm3
Surface Tension: 27.4 dyne/cm
Density: 1.96 g/cm3
Flash Point: 68.4 °C
Enthalpy of Vaporization: 40.82 kJ/mol
Boiling Point: 189.4 °C at 760 mmHg
Vapour Pressure: 0.789 mmHg at 25°C
InChI: InChI=1/C2F4O3S/c3-1(4)2(5,6)10(7,8)9-1
InChIKey: ZMSRCMWBEGLBAI-UHFFFAOYAM
Std. InChI: InChI=1S/C2F4O3S/c3-1(4)2(5,6)10(7,8)9-1
Std. InChIKey: ZMSRCMWBEGLBAI-UHFFFAOYSA-N
IUPAC Name: 3,3,4,4-Tetrafluorooxathietane 2,2-dioxide
Hazard Codes: Xi
Hazard Note: Irritant
Tetrafluoroethane beta-sultone (CAS No.697-18-7), its synonyms are 1,2-Oxathietane, 3,3,4,4-tetrafluoro-, 2,2-dioxide ; 3,3,4,4-Tetrafluoro-1,2-oxathietane 2,2-dioxide ; Tetrafluoro-1,2-oxathietane-2,2-dioxide .
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