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inquiryFormaldehyde Basic information General Description Chemical Properties Uses Product Name: Formaldehyde Synonyms: aldeideformica;BFV;CH2O;Chloditan;Chlodithan;Chlodithane;dormol;Durine CAS: 50-00-0 MF: CH2O MW: 30.03 EINECS: 200-001-8
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Formaldehyde Basic information Product Name: Formaldehyde Synonyms: METHYL ALDEHYDE;METHANONE;METHANAL;FORMALDEHYDE, CARSON-MILLON;FORMALDEHYDE, BUFFERED;FORMALDE-FRESH SOLUTION, BUF
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inquiryConditions | Yield |
---|---|
With PQQTME; calcium perchlorate; 1,8-diazabicyclo[5.4.0]undec-7-ene In acetonitrile Oxidation; | 100% |
at 370℃; under 760.051 Torr; for 1h; Reagent/catalyst; Temperature; Inert atmosphere; Flow reactor; | 100% |
With sulfuric acid Electrochemical reaction; | 100% |
Conditions | Yield |
---|---|
In benzene Ambient temperature; Irradiation; | A 100% B 100% |
phenylethane 1,2-diol
4-cyano-N,N-dimethylaniline-N-oxide
A
formaldehyd
B
4-cyano-N-methylaniline
C
benzaldehyde
D
4-cyano-N,N-dimethylaniline
Conditions | Yield |
---|---|
With chloro(5,10,15,20-tetraphenylporphyrinato)chromium(III) In acetonitrile for 0.666667h; Rate constant; Ambient temperature; Irradiation; oxygen transfer was investigated, different irradiation time; | A n/a B n/a C 100% D 100% |
Conditions | Yield |
---|---|
In benzene Ambient temperature; Irradiation; | A 100% B 100% |
Conditions | Yield |
---|---|
With hydrogenchloride; sodium hydroxide; sodium perchlorate; chlorine at 24.9℃; Mechanism; Rate constant; Equilibrium constant; multistep reaction: 1.) water, 298 deg K, 2.) water, 298 deg K; reactions under var. conditions; | A 100% B n/a C n/a |
Conditions | Yield |
---|---|
In water at 24.9℃; Rate constant; Mechanism; Thermodynamic data; Irradiation; I=0.5 mol-1 L-1; various pH; ΔH(excit.), ΔS(excit.); | A 100% B n/a |
With water In 1,4-dioxane at 25℃; | |
With water In 1,4-dioxane at 25℃; Kinetics; Mechanism; |
Conditions | Yield |
---|---|
With potassium hydroxide In methanol | A 100% B 61% |
p-nitro-N,N-dimethylaniline-N-oxide
A
formaldehyd
B
N,N-Dimethyl-4-nitroaniline
Conditions | Yield |
---|---|
With 1H-imidazole; meso-tetraphenylporphyrin iron(III) chloride; DMA-OCH3 In chloroform at 25℃; for 0.5h; | A n/a B 100% |
C6H16NO4P
A
formaldehyd
B
trans-nitrosomethane dimer
Conditions | Yield |
---|---|
With 3-chloro-benzenecarboperoxoic acid for 2h; | A n/a B 100% |
((bis(dimethylamino)phosphinyl)oxy)dimethylamine
A
formaldehyd
B
trans-nitrosomethane dimer
Conditions | Yield |
---|---|
With 3-chloro-benzenecarboperoxoic acid for 2h; | A n/a B 100% |
With 3-chloro-benzenecarboperoxoic acid for 2h; | A n/a B 100% |
1-(3,4-Dihydro-benzo[c][1,2]oxazin-1-yl)-2-methyl-propan-1-one
A
formaldehyd
B
2-isopropyl-4H-3,1-benzoxazine
Conditions | Yield |
---|---|
In 1,3,5-trimethyl-benzene Heating; | A n/a B 100% |
Conditions | Yield |
---|---|
With water; mercury ion In water Kinetics; byproducts: MeOH, H(1+); excess of Hg(2+) soln. (mol. ratio of Hg(2+)/Cr-compd. 2:1) added to soln. of Cr-compd. at 24.8°C under N2 by controlled ionic strength;Co(NH3)5F has no effect; not sepd., detected by UV; | 100% |
Conditions | Yield |
---|---|
With mercury ion In methanol; water Kinetics; byproducts: H(1+); excess of Hg(2+) soln. (mol. ratio of Hg(2+)/Cr-compd. 2:1) added to soln. of Cr-compd. in 1 M aq. MeOH at 24.8°C under N2 by controlledionic strength; Co(NH3)5F and typ of alcohols has no effect; not sepd., detected by UV; | 100% |
Conditions | Yield |
---|---|
With nitrogen; oxygen at 239.84℃; Conversion of starting material; | A 99.7% B 0.3% |
With nitrogen; oxygen at 239.84℃; Conversion of starting material; | A 98.8% B 1.2% |
With nitrogen; oxygen at 239.84℃; Conversion of starting material; | A 98.6% B 1.4% |
methane
dinitrogen monoxide
A
methanol
B
formaldehyd
C
carbon dioxide
D
carbon monoxide
E
nitrogen
Conditions | Yield |
---|---|
In neat (no solvent) Kinetics; Oxidation of CH4 by N2O in presence of catalyst (773 K): deposited Cu(2+) on carbon;; | A 0.2% B 0.3% C 99.5% D 0% E n/a |
In neat (no solvent) Kinetics; byproducts: C2H5OH (small quantity); oxidation of CH4 by N2O in presence of catalyst (773 K): deposited Ti(4+) on carbon;; | A 13.8% B 0% C 86.2% D 0% E n/a |
In neat (no solvent) Kinetics; Oxidation of CH4 by N2O in presence of catalyst (773 K): deposited Co(2+) on carbon;; | A 0% B 0% C 75% D 25% E n/a |
6,10b-dimethyl-4a,10b-dihydro-3H-naphtho<2,1-e><1,2,4>trioxine
A
formaldehyd
(1S,2R)-1,4-Dimethyl-1,2-dihydro-naphthalene-1,2-diol
Conditions | Yield |
---|---|
With acetic acid; zinc at 16℃; for 0.25h; | A n/a B 99% |
tert.-butylhydroperoxide
2,2'-azinobis-(3-ethyl-2,3-dihydrobenzothiazole-6-sulphonate) diammonium salt
A
methanol
B
formaldehyd
D
acetone
E
tert-butyl alcohol
Conditions | Yield |
---|---|
Fe(III)T4MPyP In water at 30℃; Rate constant; Kinetics; Mechanism; the catalyst Fe(III)T4MPyP is 5,10,15,20-tetra(N-methyl-4-pyridyl)-porphyrinatoiron(III) pentachloride; pH 9.2; investigation of the dependence of velocity constant on ionic strength, pH and t-butyl hydroperoxide concentration; | A 3% B n/a C 72% D 4% E 98% |
Conditions | Yield |
---|---|
With {Ru(IV)O(2,2`-bipyridine)(PEt3)}(ClO4)2 In acetonitrile at 21℃; Rate constant; Kinetics; Thermodynamic data; other Ru(IV) complex catalyst, ΔH(excit), ΔS(excit) determined; | A n/a B 98% |
With iron 5,10,15,20-tetrakis(2,4,6-trimethylphenyl)porphyrin; 3-chloro-benzenecarboperoxoic acid; 3-chlorobenzoate In dichloromethane at -50.1℃; Rate constant; also horseradish peroxidase and H2O2 as reagents; kinetic isotope effect; var. temp. and solvents; | |
With dihydrogen peroxide; sodium tartrate; 5,10,15,20-Ph4-21H,23H-porphine-p,p',p'',p'''-(SO4)4*FeCl3 In water; acetonitrile at 25℃; pH=4; oxidative N-demethylation; | A n/a B 10 % Chromat. |
Conditions | Yield |
---|---|
In tetralin at 154℃; Mechanism; Kinetics; Ea, log A, ΔH(activation), volume of activation; other solvents, other temperatures; | A n/a B 98% C 2% D n/a |
1-ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-3-quinoline carboxylic acid
A
formaldehyd
B
ammonia
C
6-fluoro-7-amino-1-ethyl-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid
Conditions | Yield |
---|---|
With potassium permanganate; cetyltrimethylammonim bromide; acetic acid In water; acetonitrile at 24.84℃; Kinetics; Catalytic behavior; Mechanism; Thermodynamic data; Activation energy; Temperature; Concentration; Solvent; UV-irradiation; | A n/a B n/a C 98% |
1-phenyl-2-piperidin-1-yl-ethanone
A
N-Formylpiperidine
B
formaldehyd
C
benzoic acid
Conditions | Yield |
---|---|
With dihydrogen peroxide In ethanol | A 14% B n/a C 96% |
With dihydrogen peroxide In ethanol | A 14% B n/a C 94% |
[2-(2-[1,3]Dithian-2-yl-1-methyl-ethoxymethoxy)-ethyl]-trimethyl-silane
A
formaldehyd
B
ethene
C
trimethylsilyl fluoride
D
2-(2-hydroxypropyl-1')-1,3-dithiane
Conditions | Yield |
---|---|
With tetrabutyl ammonium fluoride In N,N,N,N,N,N-hexamethylphosphoric triamide at 45℃; for 5h; | A n/a B n/a C n/a D 96% |
Conditions | Yield |
---|---|
molybdenum(VI) oxide In gas at 290 - 350℃; under 750.06 Torr; Thermodynamic data; Product distribution; structure sensitive oxidation with orthorhomb. or microcrystalline MoO3, further temperatures, activation energy EA; | A 95% B 5% |
With oxygen; aluminophosphate zeolite at 300℃; Product distribution; temperature, without oxygen, effect of catalysts; | |
With oxygen; vanadia at 300 - 600℃; Product distribution; further catalysts; |
2-(N,N-dimethylaminomethyl)pyrrole
A
formaldehyd
B
N-Nitrosodimethylamine
C
maleimidemonooxime
Conditions | Yield |
---|---|
With sodium nitrite In water at 25℃; for 0.05h; Product distribution; Mechanism; variation of amount of reagent and reaction period; | A n/a B 95% C n/a |
With sodium nitrite In water; acetic acid at 25℃; for 0.05h; | A n/a B 95% C n/a |
With sodium nitrite In water; acetic acid at 25℃; |
methanol
A
benzoic acid methyl ester
B
formaldehyd
C
4-methoxy-phenol
Conditions | Yield |
---|---|
With potassium carbonate at 40℃; for 1.5h; Schlenk technique; | A 95% B n/a C 90% |
Conditions | Yield |
---|---|
In acetonitrile at 70℃; for 168h; | A 94% B n/a |
lithium 2-nitropropane
diphenyliodonium bromide
A
formaldehyd
B
iodobenzene
C
biphenyl
D
2,3-dimethyl-2,3-dinitrobutane
E
2-nitro-2-phenylpropane
F
benzene
Conditions | Yield |
---|---|
In methanol at 30℃; for 48h; Mechanism; Product distribution; other diaryliodonium bromides, other times, effect of light and oxygen; | A 38% B 94% C 5% D 5% E 41% F 43% |
lithium 2-nitropropane
diphenyliodonium bromide
A
formaldehyd
B
iodobenzene
C
2-nitro-2-phenylpropane
D
benzene
Conditions | Yield |
---|---|
In methanol at 30℃; for 48h; Further byproducts given; | A 38% B 94% C 41% D 43% |
Conditions | Yield |
---|---|
With {Ru(IV)O(2,2`-bipyridine)(PPh3)}(ClO4)2 In acetonitrile at 21℃; Rate constant; Kinetics; Thermodynamic data; other Ru(IV) complex catalyst, ΔH(excit), ΔS(excit) determined; | A n/a B 94% |
With dihydrogen peroxide; FePp In ethanol at 38℃; for 0.166667h; Product distribution; borate buffer, pH 9; further educts; | |
With phosphate buffer; dihydrogen peroxide; cytochrome c at 30℃; Equilibrium constant; Rate constant; also in the presence of phosphate bilayer; |
formaldehyd
Conditions | Yield |
---|---|
In water-d2 for 0.5h; | 94% |
piperidine
Succinimide
formaldehyd
N-piperidinomethyl-succinimide
Conditions | Yield |
---|---|
With aluminum oxide In water for 0.2h; Condensation; microwave irradiation; | 100% |
With ethanol; water |
morpholine
Succinimide
formaldehyd
N-[{morpholin-1-yl}-methyl]-pyrrolidine-2,5-dione
Conditions | Yield |
---|---|
With aluminum oxide In water for 0.2h; Condensation; microwave irradiation; | 100% |
In ethanol at 60℃; for 2h; | 88% |
Conditions | Yield |
---|---|
With oxalic acid at 100 - 120℃; Eschweiler-Clarke methylation; | 100% |
With hydrogen In methanol at 100℃; under 9750.98 Torr; for 3h; Autoclave; | 97% |
With acetic acid at 30℃; for 2h; | 96% |
Conditions | Yield |
---|---|
With piperidine; acetic acid In methanol Inert atmosphere; Reflux; | 100% |
With trifluoroacetic acid; diisopropylamine 2,2,2-trifluoroacetic acid salt In tetrahydrofuran for 2h; Reflux; | 88% |
With piperidine; acetic acid In methanol; water for 6h; Reflux; | 88% |
Conditions | Yield |
---|---|
With sodium methylate for 8h; Heating; | 100% |
With methanol; sodium hydrogencarbonate | |
With sodium methylate |
Conditions | Yield |
---|---|
With potassium carbonate In water at 5℃; for 168h; | 100% |
With sodium hydroxide for 3h; Ambient temperature; | 46.4% |
With potassium carbonate In water at 5℃; for 168h; Inert atmosphere; Sealed flask; Darkness; | 32% |
formaldehyd
diethoxyphosphoryl-acetic acid ethyl ester
ethyl 2-diethoxyphosphinoylacrylate
Conditions | Yield |
---|---|
Stage #1: formaldehyd; diethoxyphosphoryl-acetic acid ethyl ester With piperidine In methanol at 80℃; for 36h; Stage #2: With toluene-4-sulfonic acid In toluene for 16h; Dean-Stark; Reflux; | 100% |
Stage #1: formaldehyd With piperidine In methanol for 0.5h; Heating; Stage #2: diethoxyphosphoryl-acetic acid ethyl ester In methanol for 70h; Heating; | 73% |
piperidine In methanol Heating; | 60% |
Conditions | Yield |
---|---|
With HCOOH (98percent) In water for 18h; Heating; | 100% |
With formic acid at 80℃; for 0.0666667h; Microwave irradiation; Neat (no solvent); | 90% |
With formic acid at 65℃; for 6h; | 89% |
Conditions | Yield |
---|---|
for 1h; Ambient temperature; | 100% |
With potassium carbonate In benzene for 6h; Heating; | 93% |
With sodium sulfate; potassium hydroxide In methanol for 6h; Reflux; | 85% |
formaldehyd
cyanuric acid
1,3,5-tri(hydroxymethyl)-1,3,5-triaza-2,4,6-cyclohexanetrione
Conditions | Yield |
---|---|
In water | 100% |
In pyridine; water for 15h; Ambient temperature; | 90% |
formaldehyd
ethanolamine
1,3,5-tris(2-hydroxyethyl)-1,3,5-triazacyclohexane
Conditions | Yield |
---|---|
In methanol at 20℃; for 16h; | 100% |
In methanol for 48h; | 86% |
With water | |
In ethanol Cyclization; | |
at 50 - 80℃; for 1h; | 92 g |
Conditions | Yield |
---|---|
Stage #1: formaldehyd; ethanolamine In water at 10℃; for 24h; Stage #2: With sulfur dioxide In water at 20℃; pH=<= 1.0; | 100% |
With water und anschliessende Saettigung mit SO2; |
formaldehyd
4-acetaminophenol
diethylamine
N-{3-[(diethylamino)methyl]-4-hydroxyphenyl}acetamide
Conditions | Yield |
---|---|
In ethanol at 80℃; for 1.5h; Microwave irradiation; | 100% |
In ethanol for 12h; Heating; | 80% |
In ethanol at 80℃; for 1h; Microwave irradiation; | 77% |
formaldehyd
diethylamine
phenylacetylene
diethyl-(3-phenyl-prop-2-ynyl)-amine
Conditions | Yield |
---|---|
With copper dichloride at 80℃; under 150.015 Torr; for 3h; Mannich reaction; | 100% |
With silver nitrate at 105℃; for 0.133333h; microwave irradiation; | 99% |
copper(l) iodide In water; dimethyl sulfoxide at 30℃; for 10h; | 98% |
Conditions | Yield |
---|---|
In toluene at 120℃; for 0.5h; | 100% |
With triethylamine In ethanol; water at 25℃; for 0.25h; Mannich Aminomethylation; Sonication; Irradiation; | 98% |
With PEG-400 for 0.0833333h; Catalytic behavior; | 95% |
Conditions | Yield |
---|---|
With potassium hydroxide In water at 50 - 52℃; for 68h; | 100% |
With potassium hydroxide for 0.05h; microwave irradiation; | 98% |
With potassium hydroxide In water at 0 - 55℃; for 36h; | 98% |
Conditions | Yield |
---|---|
With potassium carbonate In benzene at 70 - 75℃; for 3.5h; | 100% |
With barium dihydroxide In water for 40h; Ambient temperature; | 38% |
With barium dihydroxide |
Conditions | Yield |
---|---|
With sodium hydroxide; water at 25 - 40℃; for 1h; Addition; | 100% |
With water | |
for 2h; Ambient temperature; |
Conditions | Yield |
---|---|
With potassium carbonate In water at 20℃; | 100% |
With triethylamine In tetrahydrofuran; 1,4-dioxane; water a) from 4 deg C to 6 deg C, 20 min, b) RT, 40 min; | 96% |
With hydrogenchloride; sodium carbonate In water at 15 - 20℃; under 100 Torr; pH=6-7; Large scale; | 90% |
Conditions | Yield |
---|---|
With sulfuric acid Pictet-Spengler condensation; | 100% |
With sulfuric acid In water Pictet-Spengler condensation; | 100% |
With sulfuric acid under 750.075 Torr; Pictet-Spengler cyclization; Inert atmosphere; | 100% |
Conditions | Yield |
---|---|
With chloro-trimethyl-silane for 2h; Heating; | 100% |
With chloro-trimethyl-silane for 1h; Heating; | 64% |
(i), (ii) PCl5, dioxane; Multistep reaction; |
dibutyl hydrogen phosphite
formaldehyd
dibutyl (hydroxymethyl)phosphonate
Conditions | Yield |
---|---|
With potassium carbonate In cyclohexane at 20℃; for 48h; Inert atmosphere; | 100% |
triethylamine In toluene at 60℃; for 3h; | 89.1% |
With triethylamine at 90℃; for 16h; Inert atmosphere; | 76.3% |
Conditions | Yield |
---|---|
With iron(III) phosphate In acetonitrile at 80℃; for 4h; Prins condensation; | 100% |
With mesoporous SnSBA-15(5) In toluene at 89.84℃; for 6h; Prins reaction; | 96.7% |
at 150℃; | 61% |
Conditions | Yield |
---|---|
Stage #1: 3,3-Dimethylbut-1-yne With n-butyllithium In tetrahydrofuran at 0 - 20℃; Stage #2: formaldehyd In tetrahydrofuran at 20 - 65℃; for 17h; Stage #3: With water In ethyl acetate | 100% |
Stage #1: 3,3-Dimethylbut-1-yne With n-butyllithium In tetrahydrofuran; hexane at -78℃; for 0.5h; Stage #2: formaldehyd In tetrahydrofuran; hexane at -78 - 20℃; for 1h; | 98% |
With n-butyllithium; N,N,N,N,-tetramethylethylenediamine In tetrahydrofuran at -78 - 20℃; for 2h; | 97% |
Conditions | Yield |
---|---|
With palladium 10% on activated carbon; hydrogen In ethanol at 20℃; for 20h; | 100% |
With 10 mol% palladium on carbon; hydrogen In water at 20℃; under 760.051 Torr; for 36.5h; Reflux; | 99% |
With sodium dihydrogenphosphate; zinc at 30℃; for 20h; | 92% |
Conditions | Yield |
---|---|
With sodium cyanoborohydride; acetic acid In water; acetonitrile at 22℃; for 1h; pH=Ca.7; Inert atmosphere; | 100% |
With sodium dihydrogenphosphate; zinc at 30℃; for 20h; | 95% |
With sodium tetrahydroborate In 2,2,2-trifluoroethanol for 48h; Reflux; | 88% |
Conditions | Yield |
---|---|
Stage #1: n-octyne With n-butyllithium In tetrahydrofuran; hexane at -78 - 0℃; for 1h; Inert atmosphere; Stage #2: formaldehyd In tetrahydrofuran; hexane at -78 - 20℃; for 16h; Inert atmosphere; | 100% |
Stage #1: n-octyne With n-butyllithium In diethyl ether; hexane at -78℃; for 0.5h; Stage #2: formaldehyd In diethyl ether; hexane at 20℃; | 98% |
Stage #1: n-octyne With n-butyllithium In diethyl ether; hexane at -78℃; Inert atmosphere; Stage #2: formaldehyd In diethyl ether; hexane at -78 - 20℃; for 14.5h; Inert atmosphere; | 88% |
formaldehyd
1,2,4,5-tetramethylbenzene
1,4-bis(chloromethyl)-2,3,5,6-tetramethylbenzene
Conditions | Yield |
---|---|
Stage #1: formaldehyd; 1,2,4,5-tetramethylbenzene With hydrogenchloride; sodium chloride In water at 120℃; for 5h; Stage #2: With zinc(II) chloride In water for 24h; Reflux; | 100% |
With hydrogenchloride; sodium chloride In water at 120℃; for 31h; | 91% |
With hydrogenchloride; zinc(II) chloride at 90℃; for 9h; | 26% |
Conditions | Yield |
---|---|
With pyrrolidine In dichloromethane; water at 45℃; for 1h; | 100% |
With L-proline In water; N,N-dimethyl-formamide at 50℃; for 8h; | 99% |
With pyrrolidine; propionic acid In water; isopropyl alcohol at 45℃; for 4h; | 98% |
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