Conditions | Yield |
---|---|
With paraformaldehyde In hydrogen fluoride |
Conditions | Yield |
---|---|
With hydrogen fluoride |
Conditions | Yield |
---|---|
With hydrogen fluoride; trifluoroacetic acid at 50℃; under 6600.66 Torr; for 12h; Product distribution / selectivity; autoclave; | |
With 2,2,3,3,3-pentafluoropropyl trifluoroacetic acid ester; hydrogen fluoride at 50℃; under 6600.66 Torr; for 12h; Product distribution / selectivity; autoclave; | |
With 2,2,2-trifluoroethyl trifluoroacetate; hydrogen fluoride at 50℃; under 6600.66 Torr; for 12h; Product distribution / selectivity; autoclave; | |
With hydrogen fluoride at 50℃; under 6600.66 Torr; for 12h; Product distribution / selectivity; autoclave; |
2,2,3,3-tetrafluorooxetane
2,2-difluoro-3-iodopropionyl fluoride
Conditions | Yield |
---|---|
With sodium iodide | 94% |
With sodium iodide In water | |
With sodium iodide |
phenylethynylmagnesium bromide
2,2,3,3-tetrafluorooxetane
3-bromo-2,2-difluoro-1,1-bis(phenylethynyl)propan-1-ol
Conditions | Yield |
---|---|
Stage #1: phenylethynylmagnesium bromide; 2,2,3,3-tetrafluorooxetane In tetrahydrofuran at -20 - 20℃; for 20h; Inert atmosphere; Stage #2: With ammonium chloride In tetrahydrofuran; water | 91% |
Conditions | Yield |
---|---|
With sodium iodide In chloroform at 50℃; for 2h; Solvent; Cooling with ice; | 90.8% |
2,2,3,3-tetrafluorooxetane
ethanol
sodium acetate
ethyl 2,2-difluoro-3-hydroxypropanoate
Conditions | Yield |
---|---|
Stage #1: 2,2,3,3-tetrafluorooxetane; ethanol; sodium acetate at 45 - 70℃; for 2h; Reflux; Stage #2: With sulfuric acid for 8h; Reflux; Stage #3: With sodium hydrogencarbonate In water | 81.8% |
2,2,3,3-tetrafluorooxetane
diethyl ether
3-bromo-2,2-difluoropropionic acid ethyl ester
Conditions | Yield |
---|---|
With magnesium bromide at 0 - 20℃; for 3h; Inert atmosphere; | 81% |
2,2,3,3-tetrafluorooxetane
Benzyl propargyl ether
2,2-difluoro-1,1,3-tris(3-benzyloxyprop-1-ynyl)propan-1-ol
Conditions | Yield |
---|---|
Stage #1: Benzyl propargyl ether With n-butyllithium In tetrahydrofuran; hexane at -20℃; for 0.25h; Inert atmosphere; Stage #2: 2,2,3,3-tetrafluorooxetane In tetrahydrofuran; hexane at -20℃; for 2h; Inert atmosphere; Stage #3: With ammonium chloride In tetrahydrofuran; hexane; water | 78% |
2,2,3,3-tetrafluorooxetane
phenylmagnesium bromide
3-bromo-2,2-difluoro-1,1-diphenylpropan-1-ol
Conditions | Yield |
---|---|
Stage #1: 2,2,3,3-tetrafluorooxetane; phenylmagnesium bromide In tetrahydrofuran at -20 - 20℃; for 20h; Inert atmosphere; Stage #2: With ammonium chloride In tetrahydrofuran; water | 78% |
2,2,3,3-tetrafluorooxetane
para-methylphenylmagnesium bromide
3-bromo-2,2-difluoro-1,1-bis(4-methylphenyl)propan-1-ol
Conditions | Yield |
---|---|
Stage #1: 2,2,3,3-tetrafluorooxetane; para-methylphenylmagnesium bromide In tetrahydrofuran at -20 - 20℃; for 20h; Inert atmosphere; Stage #2: With ammonium chloride In tetrahydrofuran; water | 78% |
2,2,3,3-tetrafluorooxetane
trimethylsilylacetylene
2,2-difluoro-1,1,3-tris(2-trimethylsilylethynyl)propan-1-ol
Conditions | Yield |
---|---|
Stage #1: trimethylsilylacetylene With n-butyllithium In tetrahydrofuran; hexane at -20℃; for 0.25h; Inert atmosphere; Stage #2: 2,2,3,3-tetrafluorooxetane In tetrahydrofuran; hexane at -20℃; for 2h; Inert atmosphere; Stage #3: With ammonium chloride In tetrahydrofuran; hexane; water | 78% |
2,2,3,3-tetrafluorooxetane
phenylacetylene
2,2-difluoro-1,1,3-tris(2-phenylethynyl)propan-1-ol
Conditions | Yield |
---|---|
Stage #1: phenylacetylene With n-butyllithium In tetrahydrofuran; hexane at -20℃; for 0.25h; Inert atmosphere; Stage #2: 2,2,3,3-tetrafluorooxetane In tetrahydrofuran; hexane at -20℃; for 2h; Inert atmosphere; Stage #3: With ammonium chloride In tetrahydrofuran; hexane; water | 77% |
tetrahydrofuran
2,2,3,3-tetrafluorooxetane
4-iodobutyl 3-iodo-2,2-difluoropropanoate
Conditions | Yield |
---|---|
With magnesium iodide at 0 - 20℃; for 3h; Inert atmosphere; | 76% |
2,2,3,3-tetrafluorooxetane
hex-1-yne
2,2-difluoro-1,1,3-tri(hex-1-ynyl)propan-1-ol
Conditions | Yield |
---|---|
Stage #1: hex-1-yne With n-butyllithium In tetrahydrofuran; hexane at -20℃; for 0.25h; Inert atmosphere; Stage #2: 2,2,3,3-tetrafluorooxetane In tetrahydrofuran; hexane at -20℃; for 2h; Inert atmosphere; Stage #3: With ammonium chloride In tetrahydrofuran; hexane; water | 73% |
tetrahydrofuran
2,2,3,3-tetrafluorooxetane
4-bromobutyl 3-bromo-2,2-difluoropropanoate
Conditions | Yield |
---|---|
With magnesium bromide at 0 - 20℃; for 3h; Inert atmosphere; | 70% |
2,2,3,3-tetrafluorooxetane
4-methoxyphenyl magnesium bromide
3-bromo-2,2-difluoro-1,1-bis(4-methoxyphenyl)propan-1-ol
Conditions | Yield |
---|---|
Stage #1: 2,2,3,3-tetrafluorooxetane; 4-methoxyphenyl magnesium bromide In tetrahydrofuran at -20 - 20℃; for 20h; Inert atmosphere; Stage #2: With ammonium chloride In tetrahydrofuran; water | 69% |
2,2,3,3-tetrafluorooxetane
1-styrenyloxytrimethylsilane
5-bromo-4,4-difluoro-1-hydroxy-1-phenylpent-1-en-3-one
Conditions | Yield |
---|---|
Stage #1: 1-styrenyloxytrimethylsilane With methyllithium In tetrahydrofuran at -78 - 0℃; for 0.5h; Inert atmosphere; Stage #2: 2,2,3,3-tetrafluorooxetane In tetrahydrofuran at -78 - 20℃; for 2h; Inert atmosphere; Stage #3: With ammonium chloride In tetrahydrofuran; water | 66% |
2,2,3,3-tetrafluorooxetane
((1-(4-chlorophenyl)vinyl)oxy)trimethylsilane
5-bromo-4,4-difluoro-1-hydroxy-1-(4-chlorophenyl)pent-1-en-3-one
Conditions | Yield |
---|---|
Stage #1: ((1-(4-chlorophenyl)vinyl)oxy)trimethylsilane With methyllithium In tetrahydrofuran at -78 - 0℃; for 0.5h; Inert atmosphere; Stage #2: 2,2,3,3-tetrafluorooxetane In tetrahydrofuran at -78 - 20℃; for 2h; Inert atmosphere; Stage #3: With ammonium chloride In tetrahydrofuran; water | 65% |
2,2,3,3-tetrafluorooxetane
trimethyl((1-(thiophen-2-yl)vinyl)oxy)silane
5-bromo-4,4-difluoro-1-hydroxy-1-(2-thienyl)pent-1-en-3-one
Conditions | Yield |
---|---|
Stage #1: trimethyl((1-(thiophen-2-yl)vinyl)oxy)silane With methyllithium In tetrahydrofuran at -78 - 0℃; for 0.5h; Inert atmosphere; Stage #2: 2,2,3,3-tetrafluorooxetane In tetrahydrofuran at -78 - 20℃; for 2h; Inert atmosphere; Stage #3: With ammonium chloride In tetrahydrofuran; water | 64% |
2,2,3,3-tetrafluorooxetane
diethyl malonate
4,4-bis(ethoxycarbonyl)-2,2-difluorobutanamide
Conditions | Yield |
---|---|
Stage #1: diethyl malonate With sodium hydride In tetrahydrofuran at 0℃; for 0.5h; Inert atmosphere; Stage #2: 2,2,3,3-tetrafluorooxetane In tetrahydrofuran at 0 - 20℃; for 2h; Inert atmosphere; Stage #3: With ammonium chloride In tetrahydrofuran; water | 63% |
Conditions | Yield |
---|---|
Stage #1: 2,2,2-trifluoroethoxyethanol With sodium hydride In dichloromethane at 40℃; for 1h; Stage #2: 2,2,3,3-tetrafluorooxetane In diethylene glycol dimethyl ether at 0 - 20℃; for 3h; | 62% |
2,2,3,3-tetrafluorooxetane
1-p-methylphenyl-1-trimethylsiloxyethene
5-bromo-4,4-difluoro-1-hydroxy-1-(4-methylphenyl)pent-1-en-3-one
Conditions | Yield |
---|---|
Stage #1: 1-p-methylphenyl-1-trimethylsiloxyethene With methyllithium In tetrahydrofuran at -78 - 0℃; for 0.5h; Inert atmosphere; Stage #2: 2,2,3,3-tetrafluorooxetane In tetrahydrofuran at -78 - 20℃; for 2h; Inert atmosphere; Stage #3: With ammonium chloride In tetrahydrofuran; water | 60% |
Conditions | Yield |
---|---|
Stage #1: 2,2,3,3-tetrafluorooxetane; 4-Chloro-1-butanol In diethylene glycol dimethyl ether at 90 - 100℃; for 32.5h; Stage #2: With sodium carbonate In diethylene glycol dimethyl ether | 60% |
2,2,3,3-tetrafluorooxetane
1-(2-furyl)-1-(trimethylsilyloxy)ethylene
5-bromo-4,4-difluoro-1-hydroxy-1-(2-furyl)pent-1-en-3-one
Conditions | Yield |
---|---|
Stage #1: 1-(2-furyl)-1-(trimethylsilyloxy)ethylene With methyllithium In tetrahydrofuran at -78 - 0℃; for 0.5h; Inert atmosphere; Stage #2: 2,2,3,3-tetrafluorooxetane In tetrahydrofuran at -78 - 20℃; for 2h; Inert atmosphere; Stage #3: With ammonium chloride In tetrahydrofuran; water | 59% |
2,2,3,3-tetrafluorooxetane
[1-(4-methoxyphenyl)vinyloxy]trimethylsilane
5-bromo-4,4-difluoro-1-hydroxy-1-(4-methoxyphenyl)pent-1-en-3-one
Conditions | Yield |
---|---|
Stage #1: [1-(4-methoxyphenyl)vinyloxy]trimethylsilane With methyllithium In tetrahydrofuran at -78 - 0℃; for 0.5h; Inert atmosphere; Stage #2: 2,2,3,3-tetrafluorooxetane In tetrahydrofuran at -78 - 20℃; for 2h; Inert atmosphere; Stage #3: With ammonium chloride In tetrahydrofuran; water | 45% |
2,2,3,3-tetrafluorooxetane
((1-(4-fluorophenyl)vinyl)oxy)trimethylsilane
5-bromo-4,4-difluoro-1-hydroxy-1-(4-fluorophenyl)pent-1-en-3-one
Conditions | Yield |
---|---|
Stage #1: ((1-(4-fluorophenyl)vinyl)oxy)trimethylsilane With methyllithium In tetrahydrofuran at -78 - 0℃; for 0.5h; Inert atmosphere; Stage #2: 2,2,3,3-tetrafluorooxetane In tetrahydrofuran at -78 - 20℃; for 2h; Inert atmosphere; Stage #3: With ammonium chloride In tetrahydrofuran; water | 40% |
Conditions | Yield |
---|---|
With hydrogen fluoride |
2,2,3,3-tetrafluorooxetane
3-nitro-1,2,4-triazole
methyl 3-(3'-nitro-1',2',4'-triazol-1'-yl)-2,2-difluoropropionate
Conditions | Yield |
---|---|
With sodium carbonate In methanol |
The 2, 2, 3, 3-Tetrafluorooxetane has CAS registry number 765-63-9. This chemical's molecular formula is C3H2F4O and molecular weight is 130.041. What's more, its systematic name is 2, 2, 3, 3-Tetrafluorooxetane.
Physical properties about 2, 2, 3, 3-Tetrafluorooxetane are: (1)ACD/LogP: 0.28; (2)# of Rule of 5 Violations: 0; (3)#H bond acceptors: 1; (4)#H bond donors: 0; (5)#Freely Rotating Bonds: 0; (6)Polar Surface Area: 9.23 Å2; (7)Index of Refraction: 1.294; (8)Molar Refractivity: 16.12 cm3; (9)Molar Volume: 87.751 cm3; (10)Polarizability: 6.39×10-24 cm3; (11)Surface Tension: 14.067 dyne/cm; (12)Density: 1.482 g/cm3; (13)Flash Point: -74.22 °C; (14)Enthalpy of Vaporization: 22.612 kJ/mol; (15)Boiling Point: -15.774 °C at 760 mmHg; (16)Vapour Pressure: 3066.063 mmHg at 25 °C.
You can still convert the following datas into molecular structure:
(1) SMILES: FC1(F)COC1(F)F
(2) InChI: InChI=1/C3H2F4O/c4-2(5)1-8-3(2,6)7/h1H2
(3) InChIKey: OFWDLJKVZZRPOX-UHFFFAOYAZ
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