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inquiry3-BROMO-3,3-DIFLUOROPROPENE Application:3-BROMO-3,3-DIFLUOROPROPENE
Conditions | Yield |
---|---|
With potassium hydroxide |
1,1-difluoro-1,3-dibromopropane
A
3-bromo-3,3-difluropropene
B
1,1-difluoro-3-bromo-1-propene
Conditions | Yield |
---|---|
With potassium hydroxide at 115 - 130℃; Yield given. Yields of byproduct given. Title compound not separated from byproducts; | |
With potassium hydroxide In water at 120 - 160℃; Yield given. Yields of byproduct given; | |
With potassium hydroxide In water at 90 - 110℃; for 3h; |
Conditions | Yield |
---|---|
at 80℃; |
3-bromo-3,3-difluropropene
benzaldehyde
2,2-difluoro-1-phenyl-3-buten-1-ol
Conditions | Yield |
---|---|
With indium In water at 20℃; for 3h; Addition; | 100% |
With indium In N,N-dimethyl-formamide for 3h; Ambient temperature; | 99% |
With ammonium chloride; zinc In tetrahydrofuran allylation; | 84% |
Conditions | Yield |
---|---|
With indium In water for 3h; | 100% |
With zinc In tetrahydrofuran | 47% |
With indium In N,N-dimethyl-formamide |
3-bromo-3,3-difluropropene
3-phenyl-propenal
4,4-difluoro-1-phenylhexa-1,5-dien-3-ol
Conditions | Yield |
---|---|
With indium In water at 20℃; for 3h; Addition; | 100% |
With zinc In tetrahydrofuran 1.) 0 deg C to RT, 4.5 h; 2.) RT, overnight; | 74% |
Conditions | Yield |
---|---|
With indium In water at 20℃; for 3h; Addition; | 100% |
With indium In N,N-dimethyl-formamide for 3h; Ambient temperature; | 93% |
Conditions | Yield |
---|---|
With indium In N,N-dimethyl-formamide at 20℃; | 100% |
Conditions | Yield |
---|---|
With indium; lithium iodide In N,N-dimethyl-formamide | 100% |
With lithium iodide In N,N-dimethyl-formamide at 22℃; for 12h; |
Conditions | Yield |
---|---|
With indium In N,N-dimethyl-formamide for 3h; Ambient temperature; | 99% |
Conditions | Yield |
---|---|
With indium In N,N-dimethyl-formamide at 20℃; for 3h; Addition; | 99% |
3-bromo-3,3-difluropropene
tert-butyl N-(phenyl(phenylsulfonyl)methyl)carbamate
C15H19F2NO2
Conditions | Yield |
---|---|
Stage #1: 3-bromo-3,3-difluropropene With zinc(II) chloride In N,N-dimethyl-formamide at 20℃; for 1h; Stage #2: tert-butyl N-(phenyl(phenylsulfonyl)methyl)carbamate In N,N-dimethyl-formamide at 20℃; for 1h; | 99% |
Conditions | Yield |
---|---|
Stage #1: thiophenol With sodium hydride In 1,4-dioxane at 0℃; for 0.25h; Inert atmosphere; Sonication; Stage #2: 3-bromo-3,3-difluropropene In 1,4-dioxane at 0 - 20℃; for 1h; Inert atmosphere; | 99% |
Stage #1: thiophenol With sodium hydride for 0.0833333h; Inert atmosphere; Stage #2: 3-bromo-3,3-difluropropene at 20℃; for 1h; Inert atmosphere; | 99% |
3-bromo-3,3-difluropropene
Conditions | Yield |
---|---|
With palladium diacetate; triphenylphosphine In tetrahydrofuran at 40℃; for 2h; Alkylation; | 98% |
3-bromo-3,3-difluropropene
(R)-3-tert-butoxycarbonyl-4-formyl-2,2-dimethyloxazolidine
C14H23F2NO4
Conditions | Yield |
---|---|
With indium; lithium iodide In N,N-dimethyl-formamide | 98% |
Conditions | Yield |
---|---|
With indium In N,N-dimethyl-formamide for 3h; Ambient temperature; | 97% |
With indium In N,N-dimethyl-formamide at 20℃; for 3h; Addition; | 97% |
3-bromo-3,3-difluropropene
sodium diethyl methylmalonate
diethyl 2-(3,3-difluoroprop-2-enyl)isobutan-1,3-dioate
Conditions | Yield |
---|---|
With palladium diacetate; triphenylphosphine In tetrahydrofuran at 40℃; for 2h; Alkylation; | 97% |
3-bromo-3,3-difluropropene
3-(tert-butyldiphenylsilyloxy)-1-propanal
1-(tert-butyldiphenylsilyloxy)-4,4-difluoro-5-hexen-3-ol
Conditions | Yield |
---|---|
Stage #1: 3-bromo-3,3-difluropropene With indium In water at 20℃; for 0.166667h; Stage #2: 3-(tert-butyldiphenylsilyloxy)-1-propanal In tetrahydrofuran; water for 5h; | 97% |
Stage #1: 3-bromo-3,3-difluropropene With indium; lithium iodide In water at 20℃; for 0.166667h; Stage #2: 3-(tert-butyldiphenylsilyloxy)-1-propanal In tetrahydrofuran; water at 20℃; for 5h; | 97% |
With indium In tetrahydrofuran; water at 20℃; for 2h; | 93% |
With indium In tetrahydrofuran; water at 20 - 60℃; Inert atmosphere; | 90% |
With indium | 90% |
3-bromo-3,3-difluropropene
2-hydroxybromobenzene
1-bromo-2-((1’,1’-difluoroallyl)oxy)benzene
Conditions | Yield |
---|---|
With palladium diacetate; sodium hydride; triphenylphosphine In tetrahydrofuran at 0 - 40℃; for 0.5h; Catalytic behavior; Reagent/catalyst; Tsuji-Trost Allylation; Inert atmosphere; regioselective reaction; | 97% |
With palladium diacetate; sodium hydride; triphenylphosphine In tetrahydrofuran at 0 - 40℃; Tsuji-Trost Allylation; Inert atmosphere; | 83% |
3-bromo-3,3-difluropropene
Conditions | Yield |
---|---|
With bromopentacarbonylmanganese(I); N-cyclohexyl-cyclohexanamine In 1,4-dioxane at 90℃; for 22h; | 97% |
3-bromo-3,3-difluropropene
Conditions | Yield |
---|---|
With bromopentacarbonylmanganese(I); sodium acetate In 1,4-dioxane at 90℃; for 22h; | 97% |
3-bromo-3,3-difluropropene
3-methyl-1-(pyridine-2-yl)-1H-indole
Conditions | Yield |
---|---|
With bromopentacarbonylmanganese(I); sodium acetate In 1,4-dioxane at 90℃; for 22h; | 97% |
3-bromo-3,3-difluropropene
benzyloxyacetoaldehyde
1-(benzyloxy)-3,3-difluoropent-4-en-2-ol
Conditions | Yield |
---|---|
With indium In N,N-dimethyl-formamide at 20℃; for 6h; sonification; | 96% |
With indium In N,N-dimethyl-formamide at 20℃; for 5h; allylation; Sonication; | 80% |
3-bromo-3,3-difluropropene
2-bromo-4-chlorophenol
2-bromo-4-chloro-1-(1,1-difluoroallyloxy)benzene
Conditions | Yield |
---|---|
With palladium diacetate; sodium hydride; triphenylphosphine In tetrahydrofuran at 0 - 40℃; for 1h; Tsuji-Trost Allylation; Inert atmosphere; regioselective reaction; | 96% |
3-bromo-3,3-difluropropene
pivalaldehyde
4,4-Difluoro-2,2-dimethyl-hex-5-en-3-ol
Conditions | Yield |
---|---|
With n-butyllithium In tetrahydrofuran; diethyl ether; hexane; pentane at -95℃; | 95% |
3-bromo-3,3-difluropropene
methyl chloroacetate
1-Chloro-3,3-difluoro-pent-4-en-2-one
Conditions | Yield |
---|---|
With n-butyllithium In tetrahydrofuran; diethyl ether; hexane; pentane at -95℃; | 95% |
3-bromo-3,3-difluropropene
4-bromo-benzaldehyde
1-(p-bromophenyl)-2,2-difluorobut-3-en-1-ol
Conditions | Yield |
---|---|
With indium In N,N-dimethyl-formamide for 3h; Ambient temperature; | 95% |
With indium In N,N-dimethyl-formamide at 20℃; for 3h; Addition; | 95% |
furfural
3-bromo-3,3-difluropropene
2,2-difluoro-1-(furan-2-yl)but-3-en-1-ol
Conditions | Yield |
---|---|
With indium In N,N-dimethyl-formamide at 20℃; for 4h; sonification; | 95% |
With indium In N,N-dimethyl-formamide at 20℃; allylation; Sonication; | 77% |
Conditions | Yield |
---|---|
With palladium diacetate; sodium hydride; triphenylphosphine In tetrahydrofuran at 0 - 40℃; for 0.5h; Tsuji-Trost Allylation; Inert atmosphere; regioselective reaction; | 95% |
5-chloro-2H-[1,2'-bipyridin]-2-one
3-bromo-3,3-difluropropene
Conditions | Yield |
---|---|
With bromopentacarbonylmanganese(I); N-cyclohexyl-cyclohexanamine In 1,4-dioxane at 90℃; for 22h; | 95% |
3-bromo-3,3-difluropropene
Conditions | Yield |
---|---|
With bromopentacarbonylmanganese(I); sodium acetate In 1,4-dioxane at 90℃; for 22h; | 95% |
Conditions | Yield |
---|---|
With palladium diacetate; sodium hydride; triphenylphosphine In tetrahydrofuran at 0 - 40℃; Tsuji-Trost Allylation; Inert atmosphere; | 95% |
3-bromo-3,3-difluropropene
methyl 3-hydroxybenzoate
Conditions | Yield |
---|---|
With palladium diacetate; sodium hydride; triphenylphosphine In tetrahydrofuran at 0 - 40℃; Tsuji-Trost Allylation; Inert atmosphere; | 95% |
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