benzhydryl 3,3,3-triphenylpropyl ether
A
2,2-diphenylacetic acid
B
3,3,3-triphenylpropan-1-ol
Conditions | Yield |
---|---|
With naphthalene; lithium In tetrahydrofuran | A 100% B 83% |
α,α-bromodiphenylacetyl bromide
2,2-diphenylacetic acid
Conditions | Yield |
---|---|
With tetraethylammonium chloride; sodium thiosulfate In dichloromethane at 20℃; for 24h; electrochemical reaction; | 100% |
allyl 2,2-diphenylacetate
2,2-diphenylacetic acid
Conditions | Yield |
---|---|
With [2-(dicyclohexylphosphino)ethyl]trimethylammonium chloride; phenylsilane In tetrahydrofuran; water at 20℃; for 2h; Inert atmosphere; | 100% |
Conditions | Yield |
---|---|
With phosphonic Acid; methanesulfonic acid; sodium iodide In water at 95℃; for 24h; Inert atmosphere; | 99.3% |
With triethylsilane; perchloric acid In dichloromethane; water at 40℃; for 20h; | 94% |
With phosphorus; iodine weiteres Reagens: wss. Phosphorsaeure; |
Conditions | Yield |
---|---|
Stage #1: methyl 2,2-diphenylacetate With potassium hydroxide In methanesulfonic acid at 65℃; Stage #2: With hydrogenchloride In water pH=2; | 99% |
With sodium hydroxide In ethanol at 85℃; for 6h; | 85% |
With potassium hydroxide In methanol at 35℃; for 0.5h; | 83% |
With water; indium (III) iodide; silica gel for 1.5h; Hydrolysis; Irradiation; | 70% |
With sodium hydroxide In methanol; water for 3h; Reflux; |
2,2-diphenylacetic acid
Conditions | Yield |
---|---|
With iron(III) chloride In dichloromethane at 20℃; for 0.0833333h; Inert atmosphere; Green chemistry; | 99% |
Conditions | Yield |
---|---|
Stage #1: Diphenylmethane With N,N,N,N,-tetramethylethylenediamine; sodium 2,2,6,6-tetramethylpiperidide In hexane at 20℃; for 1h; Inert atmosphere; Sealed tube; Stage #2: carbon dioxide In hexane at 20℃; for 0.0833333h; Inert atmosphere; Sealed tube; | 96% |
With n-butyllithium 1.) methylcyclohexane, THF, from 0 deg C to 25 deg C, 20 h, 2.) methylcyclohexane, THF, ether; Yield given. Multistep reaction; | |
With lithium diisopropylamide 1.) THF, cyclohexane, RT, 30 min; Yield given. Multistep reaction; | |
With i-Pr2NNa*TMEDA 1.) cyclohexane, THF, 21 deg C, 30 min, 2.) cyclohexene, THF; Yield given. Multistep reaction; |
Conditions | Yield |
---|---|
With sodium hypochlorite; lithium hypochlorite In ethanol at 77℃; for 2h; | 95% |
Conditions | Yield |
---|---|
With sodium sulfate; ascorbic acid In chloroform-d1; water-d2; acetonitrile for 1h; UV-irradiation; | A 92.8% B n/a |
Conditions | Yield |
---|---|
With salcomine; tetrabutylammonium perchlorate In acetonitrile at 25℃; electrochemical reaction; | 92.6% |
With samarium; chloro-trimethyl-silane; tetra-(n-butyl)ammonium iodide In acetonitrile at 20℃; under 760.051 Torr; for 2h; Electrochemical reaction; Cooling with ice; | 66% |
(i) tBuCl, Li, Et2O, (ii) /BRN= 1900390/; Multistep reaction; |
Conditions | Yield |
---|---|
With titanium tetrachloride In 1,4-dioxane; water for 24h; Heating; | 92% |
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal In ethyl acetate for 24h; Ambient temperature; | 90% |
α,α-bromodiphenylacetyl bromide
A
2,2-diphenylacetic acid
B
2-benzhydrylidene-4,4-diphenyl-<1,3>oxathiolan-5-one
Conditions | Yield |
---|---|
With hydrogen sulfide; tetraethylammonium bromide In dichloromethane at 20℃; Mechanism; electrochemical reaction; | A 86% B 4% |
With hydrogen sulfide; tetraethylammonium bromide In dichloromethane at 20℃; electrochemical reaction; | A 86% B 4% |
(phenyl)methyl 2,2-diphenylacetate
2,2-diphenylacetic acid
Conditions | Yield |
---|---|
With methanol; sodium tetrahydroborate; nickel(II) chloride hexahydrate at 20℃; for 0.25h; chemoselective reaction; | 86% |
Conditions | Yield |
---|---|
With 1,1'-bis-(diphenylphosphino)ferrocene; [ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2; potassium tert-butylate; cesium fluoride In N,N-dimethyl-formamide at 80℃; under 760.051 Torr; for 24h; Reagent/catalyst; chemoselective reaction; | 86% |
Diphenylacetaldehyde
A
benzophenone
B
2,2-diphenylacetic acid
C
benzaldehyde
Conditions | Yield |
---|---|
With tetrafluoroboric acid diethyl ether; iodosylbenzene In dichloromethane at 20℃; for 2.5h; Inert atmosphere; | A 85% B 5% C 6 %Chromat. |
Conditions | Yield |
---|---|
In water at 80℃; for 7h; Acidic conditions; | 83% |
α,α-bromodiphenylacetyl bromide
A
2,2-diphenylacetic acid
B
Thiobenzophenon
C
2-benzhydrylidene-4,4-diphenyl-<1,3>oxathiolan-5-one
Conditions | Yield |
---|---|
With lithium sulfide; tetraethylammonium chloride In dichloromethane at 25℃; for 2h; | A 82% B 6% C 3% D 6% |
Conditions | Yield |
---|---|
With sodium hydroxide; sodium tetracarbonyl cobaltate In ethanol at 16℃; | 81.2% |
diphenylacetic acid acid 2-oxo-1,2,2-triphenylethyl ester
A
13-oxa-indeno[1,2-l]phenanthrene
B
2,2-diphenylacetic acid
Conditions | Yield |
---|---|
With air In ethanol; acetonitrile Irradiation; | A n/a B 81% |
Conditions | Yield |
---|---|
With diphenyl diselenide; dihydrogen peroxide In water at 20℃; for 6h; Green chemistry; | 80% |
Conditions | Yield |
---|---|
With poly(4-vinylpyridine) supported trifluoromethanesulfonic acid at 0 - 20℃; for 12h; | 79% |
With chlorosulfonic acid |
Conditions | Yield |
---|---|
With (4,4'-di-tert-butyl-2,2'-dipyridyl)-bis-(2-phenylpyridine(-1H))-iridium(III) hexafluorophosphate; sodium carbonate; caesium carbonate In N,N-dimethyl-formamide at 25 - 30℃; for 26h; Schlenk technique; Glovebox; Sealed tube; Irradiation; | 79% |
3-(diphenylmethyl)-5,6-dihydro-1,4,2-dioxazine
2,2-diphenylacetic acid
Conditions | Yield |
---|---|
With hydrogenchloride for 18h; Heating; | 78% |
With hydrogenchloride In methanol at 65℃; for 10h; |
Conditions | Yield |
---|---|
With manganese; dichlorobis(trimethylphosphine)nickel In N,N-dimethyl-formamide at 100℃; under 760.051 Torr; for 24h; Reagent/catalyst; Temperature; Schlenk technique; | 78% |
Conditions | Yield |
---|---|
In ammonia for 5h; Phenylation; Irradiation; | 77% |
(Diphenylacetyl)(2,4-dioxo-5,5-diphenyl-3-oxazolidinyl)carbamidsaeure-tert-butylester
A
2,2-diphenylacetic acid
B
2-(Hydroxydiphenylacetyl)hydrazincarbonsaeure-tert-butylester
Conditions | Yield |
---|---|
With sodium hydroxide In 1,4-dioxane; ethanol for 1h; Heating; | A 75% B 67% |
carbon dioxide
diphenylchloromethane
A
Diphenylmethane
B
2,2-diphenylacetic acid
Conditions | Yield |
---|---|
With salcomine; tetrabutylammonium perchlorate; water In acetonitrile at 25℃; electrochemical reaction; | A 72.3% B 24.7% |
2,2-diphenylacetic acid
Conditions | Yield |
---|---|
Stage #1: 2,2-diphenyl-N-(quinolin-8-yl)acetamide With ozone In dichloromethane at -78℃; Inert atmosphere; Stage #2: With lithium hydroxide monohydrate; dihydrogen peroxide In tetrahydrofuran; water at 20℃; for 24h; Inert atmosphere; | 71% |
2-<1'-(Diphenylacetoxy)-2',2'-diphenylethenyl>-1-methyl-benzimidazole
A
2,2-diphenylacetic acid
B
2-(Diphenylacetyl)-1-methylbenzimidazole
Conditions | Yield |
---|---|
With potassium hydroxide In methanol for 1h; Heating; | A 0.3 g B 70% |
2,2-diphenylacetic acid
1-(2-Benzoyl-6H-[1,3]thiazin-5-yl)-ethanone
Conditions | Yield |
---|---|
With methanesulfonyl chloride; triethylamine In dichloromethane for 15h; Ambient temperature; | 100% |
Conditions | Yield |
---|---|
In 1,2-dimethoxyethane at 20℃; for 96h; | 100% |
Conditions | Yield |
---|---|
With dmap; diisopropyl-carbodiimide In dichloromethane at 0 - 20℃; | 100% |
With dmap; triethylamine; diisopropyl-carbodiimide In dichloromethane | |
Stage #1: (E/Z)-2-buten-1-ol; 2,2-diphenylacetic acid With dmap; triethylamine In dichloromethane at 0℃; for 0.25h; Stage #2: With diisopropyl-carbodiimide In dichloromethane at 0 - 20℃; for 16h; |
2,2-diphenylacetic acid
3-Phenylpropan-1-amine
N-(3-phenylpropyl)diphenylacetamide
Conditions | Yield |
---|---|
With dmap; benzenesulfonic anhydride In dichloromethane at 20℃; for 1h; | 100% |
Stage #1: 2,2-diphenylacetic acid With dmap; nicotinic anhydride In dichloromethane at 0℃; for 0.166667h; Stage #2: 3-Phenylpropan-1-amine In dichloromethane at 0℃; for 1h; | 94% |
Stage #1: 2,2-diphenylacetic acid With dmap; 1,1'-carbonyldiimidazole In dichloromethane at 20℃; for 0.333333h; Stage #2: 3-Phenylpropan-1-amine In dichloromethane at 20℃; for 5h; | 64% |
Stage #1: 2,2-diphenylacetic acid With dmap; 1,1'-carbonyldiimidazole In dichloromethane at 20℃; for 0.5h; Stage #2: 3-Phenylpropan-1-amine In dichloromethane at 20℃; for 4h; Further stages.; | 63% |
2,2-diphenylacetic acid
rac-methylbenzylamine
N-(α-phenylethyl)diphenylacetamide
Conditions | Yield |
---|---|
With dmap; benzenesulfonic anhydride In dichloromethane at 20℃; for 1h; | 100% |
Stage #1: 2,2-diphenylacetic acid With dmap; nicotinic anhydride In dichloromethane at 0℃; for 0.166667h; Stage #2: rac-methylbenzylamine In dichloromethane at 0℃; for 1h; | 98% |
With dmap In dichloromethane at 20℃; for 1h; | 96% |
2,2-diphenylacetic acid
phenethylamine
N-phenethyl-2,2-diphenylacetamide
Conditions | Yield |
---|---|
With dmap In chloroform at 25℃; for 1h; | 100% |
Stage #1: 2,2-diphenylacetic acid With fur-2-ylboronic acid In dichloromethane for 0.166667h; Molecular sieve; Inert atmosphere; Stage #2: phenethylamine In dichloromethane at 20℃; for 24h; Molecular sieve; Inert atmosphere; | 17% |
Conditions | Yield |
---|---|
With thionyl chloride | 99% |
With thionyl chloride In benzene for 2h; Reflux; | 96% |
With thionyl chloride for 1h; Heating; | 90% |
Conditions | Yield |
---|---|
Stage #1: 2,2-diphenylacetic acid With ethanaminium,N-(difluoro-λ4-sulfanylidene)-N-ethyl-,tetrafluoroborate In ethyl acetate at 21℃; for 2h; Inert atmosphere; Stage #2: morpholine In ethyl acetate at 21℃; for 1h; Inert atmosphere; | 99% |
With pyridine; 4-chloro-3-nitro-chromen-2-one 1.) DMF, 18-20 deg C, 15 min, 2.) DMF, 30 min; Multistep reaction; |
3-Phenylpropenol
2,2-diphenylacetic acid
Diphenylessigsaeure-<3-phenyl-allylester>
Conditions | Yield |
---|---|
With dmap; picryl fluoride In acetonitrile for 6h; Ambient temperature; | 99% |
Conditions | Yield |
---|---|
In tetrachloromethane for 15h; Ambient temperature; | 99% |
2,2-diphenylacetic acid
4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane
Conditions | Yield |
---|---|
In neat (no solvent) at 30℃; Inert atmosphere; Schlenk technique; Glovebox; chemoselective reaction; | 99% |
With [ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2 In neat (no solvent) at 60℃; for 24h; | |
With (4-Me)Triaz(NHPiPr2)2Mn(CO)2Br In toluene at 25℃; for 6h; Catalytic behavior; Inert atmosphere; chemoselective reaction; | > 99 %Spectr. |
Conditions | Yield |
---|---|
Stage #1: 2,2-diphenylacetic acid With oxalyl dichloride In dichloromethane; N,N-dimethyl-formamide at 25℃; Stage #2: methanol In dichloromethane at 25℃; Cooling with ice; | 98.7% |
With oxalyl dichloride; N,N-dimethyl-formamide In dichloromethane at 25℃; Cooling with ice; | 98.7% |
With sulfuric acid Reflux; | 93% |
2,4-dimethyl-3-pentyl chloroformate
2,2-diphenylacetic acid
Diphenyl-acetic acid 1-isopropyl-2-methyl-propyl ester
Conditions | Yield |
---|---|
With triethylamine; dmap In dichloromethane at 0℃; for 1h; | 98% |
Conditions | Yield |
---|---|
With trimethylamine-N-oxide; copper(l) chloride In acetonitrile at 60℃; for 24h; Mechanism; Product distribution; other diaryl acetic acid, copper(I) or copper(II) chloride; | 98% |
With 1H-imidazole; sodium periodate; 5,10,15,20-tetrakis-(4-aminophenyl) manganese(III) porphyrin chloride In water; acetonitrile at 25℃; for 0.833333h; Reagent/catalyst; Solvent; | 97% |
With oxygen; tetra-N-butylammonium tribromide In ethyl acetate at 20℃; for 23h; Catalytic behavior; Irradiation; | 96% |
2,2-diphenylacetic acid
diphenylacetic-2-t acid
Conditions | Yield |
---|---|
With sodium hydroxide; tritium oxide for 64h; Heating; | 98% |
N-methylene-tert-butylamine
2,2-diphenylacetic acid
acetylenedicarboxylic acid diethyl ester
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 48h; | 98% |
2,2-diphenylacetic acid
N-benzyloxycarbonyl-(2S,4R)-4-hydroxyproline benzyl ester
(2S,4R)-dibenzyl 4-(2,2-diphenylacetoxy)pyrrolidine-1,2-dicarboxylate
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 0 - 20℃; Inert atmosphere; | 98% |
2,2-diphenylacetic acid
ethyl 2-chloro-3-oxo-butyrate
ethyl 2-(2,2-diphenylacetoxy)-3-oxobutanoate
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃; for 17h; | 98% |
With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃; for 17h; | 98% |
With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃; for 17h; | 98% |
2,2-diphenylacetic acid
tert-butyl 4-((2-(hydrazinecarbonyl)benzo[b]thiophen-3-yl)oxy)piperidine-1-carboxylate
tert-butyl 4-((2-(2-(2,2-diphenylacetyl)hydrazinecarbonyl)benzo[b]thiophen-3-yl)oxy)piperidine-1-carboxylate
Conditions | Yield |
---|---|
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In tetrahydrofuran; N,N-dimethyl-formamide at 20℃; for 18h; | 98% |
Conditions | Yield |
---|---|
With C58H34F18O6P2Ru; tris(pentafluorophenyl)borate; acenaphthene In toluene at 140℃; for 4h; Inert atmosphere; | 98% |
Conditions | Yield |
---|---|
With 1,3-(2,2-dimethyl)propanedinitrite In tert-butyl alcohol at 80℃; for 6h; | 98% |
2,2-diphenylacetic acid
carbonic acid dimethyl ester
methyl 2,2-diphenylacetate
Conditions | Yield |
---|---|
With sulfuric acid at 80 - 85℃; for 3.5h; Neat (no solvent); | 97.5% |
Conditions | Yield |
---|---|
Ru(η3-CH2=C(Me)CH2)2 In toluene at 65℃; for 20h; | 97% |
2,2-diphenylacetic acid
2-Benzoyl-6H-[1,3]thiazine-5-carboxylic acid methyl ester
Conditions | Yield |
---|---|
With methanesulfonyl chloride; triethylamine In dichloromethane for 15h; Ambient temperature; | 97% |
1. | orl-rat LD50:5540 mg/kg | GNAMAP Gigiena Naselennykh Mest. Hygiene in Populated Places. 17 (1978),48. | ||
2. | orl-mus LD50:3200 mg/kg | GNAMAP Gigiena Naselennykh Mest. Hygiene in Populated Places. 17 (1978),48. | ||
3. | ipr-mus LD50:500 mg/kg | FRPSAX Farmaco, Edizione Scientifica. 13 (1958),286. | ||
4. | scu-mus LD50:400 mg/kg | AIPTAK Archives Internationales de Pharmacodynamie et de Therapie. 116 (1958),154. |
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