Conditions | Yield |
---|---|
With mercury(II) oxide |
acetic anhydride
A
mercury(II) diacetate
B
ammonium acetate
C
acetic acid
Conditions | Yield |
---|---|
Heating / reflux; | |
In water at 50℃; | |
at 50℃; |
mercuric carbonate
mercury(II) diacetate
Conditions | Yield |
---|---|
With acetic acid In acetic acid | |
With acetic acid In acetic acid aq. acetic acid; |
mercury(II) diacetate
Conditions | Yield |
---|---|
With acetic acid In acetic acid on water bath; filtered, cooled, washed with ethyl acetate, recrystd., drying above CaCl2 in vacuum; | |
With acetic acid In acetic acid washed with chloroform, drying above caustic soda in vacuum; | |
With acetic acid In acetic acid aq. acetic acid; on water bath; filtered, cooled, washed with ethyl acetate, recrystd., drying above CaCl2 in vacuum; | |
With glacial acetic acid In acetic acid washed with chloroform, drying above caustic soda in vacuum; |
Conditions | Yield |
---|---|
In not given byproducts: KNO3; | |
In not given byproducts: KNO3; |
mercury(II) diacetate
Conditions | Yield |
---|---|
With CH3COOH; H2O2; nitric acid In not given refluxed 40°C, mixed with H2O2, 80°C 30 min, evaporated at ambient temp. and vacuum; | |
With dihydrogen peroxide; acetic acid; nitric acid In not given refluxed 40°C, mixed with H2O2, 80°C 30 min, evaporated at ambient temp. and vacuum; |
Conditions | Yield |
---|---|
In acetic acid | >99 |
In acetic acid | >99 |
mercury(II) diacetate
Conditions | Yield |
---|---|
With acetic anhydride 4-5-fold excess of (CH3CO)2O; | |
With acetic anhydride 4-5-fold excess of (CH3CO)2O; |
Conditions | Yield |
---|---|
With nitric acid In water Hg(NO3)2 acidified with HNO3; | |
With HNO3 In water Hg(NO3)2 acidified with HNO3; |
Conditions | Yield |
---|---|
In further solvent(s) all manipulations by Schlenk technique; no reaction even in molar ratio of Hg compd.:org. compd. 1:2, only dismutation; |
Conditions | Yield |
---|---|
In pyridine disproportion in pyridine; | |
In water Irradiation (UV/VIS); heating; | |
In water Irradiation (UV/VIS); heating; | |
In pyridine disproportion in pyridine; |
mercury(II) diacetate
Conditions | Yield |
---|---|
With acetic anhydride In acetic anhydride |
Conditions | Yield |
---|---|
In acetic acid Irradiation (UV/VIS); | |
In acetic acid Irradiation (UV/VIS); |
(HgCN)(1+)*(CH3CO2)(1-)={HgCN}CH3CO2
A
mercury(II) diacetate
Conditions | Yield |
---|---|
With H2O | |
With water |
Conditions | Yield |
---|---|
In water Kinetics; equil.; equil. constant given;; | |
In water Kinetics; equil.; equil. constant given;; |
Conditions | Yield |
---|---|
In not given |
Conditions | Yield |
---|---|
In benzene under N2, kept for several hours at room temp.; |
Conditions | Yield |
---|---|
In dichloromethane Electrolysis; controlled potential oxidative electrolysis at a Hg pool electrode in CH2Cl2 at 20°C in the presence of 0.1 M Bu4NClO4; further unidentified products; not isolated; |
[(acetoxymercuriothio)methyl]triethylsilane
B
mercury(II) diacetate
Conditions | Yield |
---|---|
In benzene dilute soln.; |
C2H3O2(1-)*C4H11O3SSi(1-)*Hg(2+)
B
mercury(II) diacetate
Conditions | Yield |
---|---|
In benzene dilute soln.; |
C2H3O2(1-)*C6H15O3SSi(1-)*Hg(2+)
B
mercury(II) diacetate
Conditions | Yield |
---|---|
In benzene dilute soln.; |
C2H3O2(1-)*C5H13O3SSi(1-)*Hg(2+)
B
mercury(II) diacetate
Conditions | Yield |
---|---|
In benzene dilute soln.; |
Conditions | Yield |
---|---|
In benzene dilute soln.; |
B
mercury(II) diacetate
Conditions | Yield |
---|---|
In not given decomp. in soln.;; |
mercury(II) diacetate
2,3,6-tri-O-benzoyl-4-deoxy-α-D-xylo-hexopyranosyl chloride
1-O-acetyl-2,3,6-tri-O-benzoyl-4-deoxy-β-D-xylo-hexopyranose
Conditions | Yield |
---|---|
In acetic acid for 1h; Ambient temperature; | 100% |
Conditions | Yield |
---|---|
In dichloromethane for 3h; Ambient temperature; | A n/a B 100% |
Conditions | Yield |
---|---|
trifluoroborane diethyl ether In methanol 0.2 Mol catalysts, in 0.2 molar soln., 24h, 50°C; | 100% |
trifluoroborane diethyl ether In methanol 0.2 Mol catalysts, in 0.2 molar soln., 24h, 50°C; | 100% |
perchloric acid In methanol 0.34 Mol HClO4, in 0.2 molar soln., 70h, 50°C; | 60% |
4-methylbenzenetrifluorosilane
mercury(II) diacetate
p-CH3-C6H4-Hg-CH3CO2
Conditions | Yield |
---|---|
In benzene addn. of 4-CH3-PhSiF3 to suspn. of HgAc2, mixt. heated (5 min, 80°C); cooled, filtered; | 100% |
mercury(II) diacetate
Conditions | Yield |
---|---|
In tetrahydrofuran byproducts: Hg, dme; react. at room temp. for 16 h under N2; suspn. filtered, filter washed (THF), filtrate and washings evapd. (vac.); elem. anal.; | 100% |
Conditions | Yield |
---|---|
In benzene byproducts: F3SiOCOCH3; addn. of PhSiF3 to suspn. of HgAc2, mixt. heated ( 10-15 min, 80°C); cooled, filtered; | 100% |
In benzene byproducts: F3SiOCOCH3; suspn. of HgAc2 in benzene treated with PhSiF3, after 10-15 min heated to boiling; crystn. upon cooling; | 100% |
In benzene byproducts: F3SiOCOCH3; react. of starting materials in soln. at 25°C for 2h; | 99% |
bicyclo[1.1.0]butane
mercury(II) diacetate
1-acetoxymercuri-3-acetoxycyclobutane
Conditions | Yield |
---|---|
In dichloromethane addn. of bicylobutane to suspn. of Hg(OAc)2 in CH2Cl2 (stirring), stirring (30 min); removal of solvent (evapn.); | 100% |
ortho-biphenylenemercury trimer
mercury(II) diacetate
C12H8(HgO2CCH3)2
Conditions | Yield |
---|---|
In methanol the biphenylenemercury suspensed in boiling methanol; mercuric acetate added until all the trimer had dissolved; a little more trimer was added; filtration; evaporation to a small volume; crystals washed quickly withcold glacial acetic acid and copious amounts of distilled water; dried at 80°C; elem. anal.; | 100% |
In 1,2,5-trimethyl-benzene refluxed in boiling mesitylene for 30 min; solvent was partially evaporated; cooled; further evaporation of the filtrate; | 0% |
Conditions | Yield |
---|---|
In methanol addn. of soln. of 1 mmol Hg acetate in methanol to soln. of 1 mmol triazene in methanol; stirring mixture at ambient temp. for 12 h;; washing with ether and water;; | 100% |
HN4CN3(H)C6H4Cl
mercury(II) diacetate
[Hg(N4C)N=NNC6H4Cl](n)
Conditions | Yield |
---|---|
In methanol addn. of soln. of 1 mmol Hg acetate in methanol to soln. of 1 mmol triazene in methanol; stirring mixture at ambient temp. for 12 h;; washing with ether and water;; | 100% |
Conditions | Yield |
---|---|
In methanol addn. of soln. of 1 mmol Hg acetate in methanol to soln. of 1 mmol triazene in methanol; stirring mixture at ambient temp. for 12 h;; washing with ether and water;; | 100% |
(triethylsilyl)methanethiol
mercury(II) diacetate
[(acetoxymercuriothio)methyl]triethylsilane
Conditions | Yield |
---|---|
In tetrahydrofuran byproducts: CH3COOH; stirring (1 h, room temp.); solvent driving off (rotary evaporator), residue diln. (benzene), unchanged Hg-acetate filtration off, benzene and acetic acid evapn. (vac.) from filtrate, residue (thick oil) crystn. during 1 d; elem. anal.; | 100% |
mercury(II) diacetate
Conditions | Yield |
---|---|
In chloroform | 100% |
mercury(II) diacetate
Conditions | Yield |
---|---|
In chloroform | 100% |
3,4,5-trimethoxy(N-tert-butylcarbamoyl)benzene
mercury(II) diacetate
Conditions | Yield |
---|---|
With HOAc In ethanol; water air and moisture free atmosphere; refluxing (5 h), stirring (overnight),KCl soln. (H2O) addn., stirring (10 min); filtering, washing (H2O), drying (70°C); elem. anal.; | 100% |
Conditions | Yield |
---|---|
With triethylamine In methanol for 0.75h; | 100% |
mercury(II) diacetate
Conditions | Yield |
---|---|
Stage #1: N-(3,5-bis{[ethyl(methyl)amino]methyl}phenyl)hexadecanamide; mercury(II) diacetate In ethanol for 24h; Inert atmosphere; Reflux; Stage #2: lithium chloride In ethanol for 0.25h; Inert atmosphere; Reflux; | 100% |
Conditions | Yield |
---|---|
Stage #1: C37H56N6O7Si; acetic acid In dichloromethane at 20℃; for 6h; Stage #2: mercury(II) diacetate In dichloromethane at 0℃; for 2h; | 100% |
mercury(II) diacetate
Conditions | Yield |
---|---|
In methanol; acetonitrile byproducts: acetic acid; soln. of Hg salt in MeOH added to soln. of ligand (2 equiv.) in MeCN; heated to 70°C; stirred for 1 h; cooled to ambient temp.; Et2O layered onto filtrate; crystd. for several d; collected by filtration; washed with Et2O; dried in vac.; elem. anal.; | 99.4% |
Conditions | Yield |
---|---|
In ethanol for 0.166667h; Heating; Yields of byproduct given; | A n/a B 99% |
Conditions | Yield |
---|---|
In ethanol for 0.25h; Heating; Yields of byproduct given; | A n/a B 99% |
mercury(II) diacetate
Conditions | Yield |
---|---|
In acetic acid for 0.5h; Ambient temperature; | 99% |
isopropyl aldehyde dithiophenylacetal
mercury(II) diacetate
(1-Acetoxy-isobutyl)-phenyl-sulfid
Conditions | Yield |
---|---|
In acetic acid Ambient temperature; | 99% |
Conditions | Yield |
---|---|
In methanol mixing MeOH (or EtOH) solns. of stoich. amts. of Hg(OAc)2 and carboxylic acid; elem. anal.; | 99% |
(η5-pentamethylcyclopentadienyl)(η5-indenyl)ruthenium(II)
mercury(II) diacetate
Conditions | Yield |
---|---|
In diethyl ether; ethanol under N2; mixt. Ru-complex, 3 equiv Hg-compd., EtOH and Et2O stirred (ambient temp., 12 h); evapn. (reduced pressure), washed (hexane), solid dissolved in CH2Cl2, filtered (Celite), evapn. (reduced pressure), elem. anal.; | 99% |
Conditions | Yield |
---|---|
In 1,4-dioxane; methanol salen metal complex dissolved in hot 1,4-dioxane; to this soln. added mercury salt dissolved in MeOH with stirring; mixt. heated at 120°Cfor 5 h; cooled; soln. concd.; crystals were obtained; elem. anal.; | 99% |
mercury(II) diacetate
5,5-dimethyl-2-(3-methyl-3-butenyl)-1,3-cyclohexanedione
2-chloromercurymethyl-2,7,7-trimethyl-3,4,5,6,7,8-hexahydro-2H-benzopyran-5-one
Conditions | Yield |
---|---|
With potassium chloride In tetrahydrofuran; water to a soln. of mercuric acetate in THF is added the olefin-compd. at room temp. under stirring for 3-5 h., a soln. of KCl in water is added and the soln. is stirred for 5 min.; the soln. is diluted with water and extracted with CH2Cl2, the extract is dried over anhydrous Na2SO4 and the solvent is evaporated under red. pressure, benzene is added to the residue and then evaporated, crystn. from AcOEt; | 99% |
mercury(II) diacetate
Conditions | Yield |
---|---|
With diisopropylethylamine In chloroform-d1; d(4)-methanol titration of porphyrine by Hg(OAc)2; monitored by UV; solvent evapd., solid dissolved in CH2Cl2, excess of mercury salt removed by filtration through celite, precipitated with pentane; elem. anal.; | 99% |
In pyridine room temp.; 15 min; monitored by UV; solvent evapd., solid dissolved in CH2Cl2, excess of mercury salt removed by filtration through celite, precipitated with pentane; elem. anal.; | 82% |
1-vinyl-4,5,6,7-tetrahydroindole-2-carbonitrile
mercury(II) diacetate
2-acetoxy-2-(2-cyano-4,5,6,7-tetrahydroindol-1-yl)ethylmercury acetate
Conditions | Yield |
---|---|
In acetonitrile by a react. in dry CH3CN at 60°C for 4 h; | 99% |
3-vinyl-4,5-dihydro-3H-benzo[e]indole-2-carbaldehyde
mercury(II) diacetate
C6H4C2H4C4HNCHO2CCH3CH2HgO2CCH3CHO
Conditions | Yield |
---|---|
In acetonitrile by a react. in dry CH3CN at 35°C for 2 h; | 99% |
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