Conditions | Yield |
---|---|
With disulfur dichloride; iron(III) chloride In neat (no solvent) addn. of a mixt. of 140 g PCl3 and 1.7 g S2Cl2 drop by drop to a hot mixt. of 160 g PSCl3, 2 g anhydrous FeCl3 and 38 g S on stirring and refluxing (4.5 h); refluxing for 1 h, distg. off PSCl3;; | 100% |
In neat (no solvent) react. molten S with PCl3 at 124-126 °C at ambient pressure; use of a catalyst formed on melting S with active carbon and boiling in PSCl3 at 200 °C;; | |
disulfur dichloride In not given react. with S2Cl2 as catalyst;; |
phosphorus pentachloride
A
trichlorothiophosphine
Conditions | Yield |
---|---|
In neat (no solvent) react. on heating under blazing up;; |
phosphorus pentachloride
A
trichlorothiophosphine
Conditions | Yield |
---|---|
In neat (no solvent) react. on heating under blazing up;; |
phosphorus pentachloride
A
trichlorothiophosphine
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: thiosulfate; react. on heating;; |
thionyl chloride
A
disulfur dichloride
B
trichlorothiophosphine
C
phosphorus pentachloride
D
sulfur dioxide
E
phosphorus trichloride
Conditions | Yield |
---|---|
In neat (no solvent) excess of SOCl2; 180°C;; | |
In neat (no solvent) excess of SOCl2; 180°C;; |
sulfur dioxide
phosphorus trichloride
A
trichlorothiophosphine
B
sulfur
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: POCl3; decompn. of SO2- and PCl3-vapours in a calcinating tube;; formation of POCl3, PSCl3 and a small amount of S;; | |
In neat (no solvent) byproducts: POCl3; decompn. of SO2- and PCl3-vapours in a calcinating tube;; formation of POCl3, PSCl3 and a small amount of S;; |
sulfur dioxide
phosphorus trichloride
A
trichlorothiophosphine
B
trichlorophosphate
Conditions | Yield |
---|---|
tetramethyl ammonium-pyrosulfite 50°C; | |
phosphorus tribromide 50°C; | |
phosphorus(V) oxybromide 50°C; |
disulfur dichloride
A
trichlorothiophosphine
B
trichlorophosphate
C
phosphorus trichloride
Conditions | Yield |
---|---|
With silica gel In neat (no solvent) byproducts: SiCl4; react. of Ca3(PO4)2 with S2Cl2 at 1000 °C in presence of SiO2;; after 1 h 9.5 % phosphate are caused to react.;; | |
In neat (no solvent) react. of Ca3(PO4)2 with S2Cl2 at 1000 °C;; after 1 h 19.5 % phosphate are caused to react.;; | |
In neat (no solvent) react. of Ca3(PO4)2 with S2Cl2 at 1000 °C;; after 1 h 19.5 % phosphate are caused to react.;; | |
With SiO2 In neat (no solvent) byproducts: SiCl4; react. of Ca3(PO4)2 with S2Cl2 at 1000 °C in presence of SiO2;; after 1 h 9.5 % phosphate are caused to react.;; |
disulfur dichloride
A
trichlorothiophosphine
B
sulfur
C
phosphorus trichloride
Conditions | Yield |
---|---|
In neat (no solvent) addn. of P (excess) to boiling S2Cl2;; |
Conditions | Yield |
---|---|
In neat (no solvent) addn. of P to boiling S2Cl2;; | |
In neat (no solvent) react. at boiling temp.;; | |
With Fe or Al In neat (no solvent) heating P with S2Cl2 in presence of Fe or Al;; | |
In neat (no solvent) heating P with S2Cl2;; |
thionyl chloride
phosphorus trichloride
A
trichlorothiophosphine
B
phosphorus pentachloride
C
trichlorophosphate
Conditions | Yield |
---|---|
In neat (no solvent) slowly at 80-160°C;; POCl3 only supposed;; |
thionyl chloride
phosphan
A
hydrogenchloride
B
trichlorothiophosphine
D
phosphorus sulfide
E
trichlorophosphate
Conditions | Yield |
---|---|
In neat (no solvent) room temp.;; further unidentified liquid products;; |
thionyl chloride
A
disulfur dichloride
B
trichlorothiophosphine
C
sulfur dioxide
E
sulfur
Conditions | Yield |
---|---|
In neat (no solvent) 100-150°C;; | A 0% B n/a C n/a D 0% E n/a |
In neat (no solvent) 100-150°C;; | A 0% B n/a C n/a D 0% E n/a |
thionyl chloride
A
disulfur dichloride
B
trichlorothiophosphine
C
sulfur dioxide
D
sulfur
Conditions | Yield |
---|---|
In neat (no solvent) 100-150°C;; | A 0% B n/a C n/a D n/a |
thionyl chloride
A
disulfur dichloride
B
trichlorothiophosphine
C
phosphorus pentachloride
D
sulfur dioxide
E
phosphorus trichloride
Conditions | Yield |
---|---|
In neat (no solvent) excess of SOCl2; 180°C;; | |
In neat (no solvent) excess of SOCl2; 180°C;; |
phosphorus trichloride
trichlorothiophosphine
Conditions | Yield |
---|---|
With sulfur at 76°C, in common pressure; | 0% |
With sulfur; barium sulfide in autoclave at 150°C for 4-5 h; | >99 |
With sulfur; calcium(II) sulfide in autoclave at 150°C for 4-5 h; | >99 |
disulfur dichloride
phosphorus trichloride
A
trichlorothiophosphine
B
phosphorus pentachloride
Conditions | Yield |
---|---|
In neat (no solvent) 6h, 160°C;; | A >99 B >99 |
In neat (no solvent) 6h, 160°C;; | A >99 B >99 |
sulfuryl dichloride
phosphorus trichloride
A
trichlorothiophosphine
B
trichlorophosphate
Conditions | Yield |
---|---|
In neat (no solvent) simultaneous formation of POCl3 and PSCl3 via reaction of PCl3 with SO2Cl2;; isolation via fractionation;; | |
In not given react. with SO2Cl2;; fractional distn.;; | |
In not given react. with SO2Cl2;; fractional distn.;; |
disulfur dichloride
A
trichlorothiophosphine
B
trichlorophosphate
C
phosphorus trichloride
Conditions | Yield |
---|---|
With silica gel In neat (no solvent) byproducts: SiCl4; react. of Ca(PO3)2 with S2Cl2 at 1000 °C in presence of SiO2;; | |
With SiO2 In neat (no solvent) byproducts: SiCl4; react. of Ca(PO3)2 with S2Cl2 at 1000 °C in presence of SiO2;; |
disulfur dichloride
phosphorus(III) oxide
A
trichlorothiophosphine
B
sulfur dioxide
C
trichlorophosphate
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: S; vigorous reaction;; |
disulfur dichloride
A
trichlorothiophosphine
B
sulfur
C
phosphorus trichloride
Conditions | Yield |
---|---|
In neat (no solvent) in coldness under inflammation;; |
phosphorus pentachloride
potassium thioacyanate
A
disulfur dichloride
B
trichlorothiophosphine
D
cyanogen chloride
Conditions | Yield |
---|---|
In neat (no solvent) haeting at lower temp.; formation of CNCl, PSCl3, KCl and a small amount of S2Cl2;; |
phosphorus pentachloride
potassium thioacyanate
A
trichlorothiophosphine
C
cyanogen chloride
Conditions | Yield |
---|---|
heating; | |
heating; |
phosphorus pentachloride
A
trichlorothiophosphine
B
thionyl chloride
D
trichlorophosphate
Conditions | Yield |
---|---|
In neat (no solvent) heating PbS2O3 (dryed at 400 °C) with a reflux condenser; react. starting without heating, react. accelerated on heating; formation of POCl3, SOCl2, PSCl3 and PbCl2 as residue;; |
trichlorophosphate
A
trichlorothiophosphine
B
phosphoric acid
Conditions | Yield |
---|---|
In neat (no solvent) react. with P2S5 in a sealing tube at 150 °C;; | |
In neat (no solvent) heating in a sealing tube at 150 °C;; | |
In neat (no solvent) react. with P2S5 in a sealing tube at 150 °C;; |
phosphorus pentachloride
trichlorothiophosphine
Conditions | Yield |
---|---|
With metal sulfide In not given byproducts: metal chloride; react. with metal sulfides forming PSCl3 and corresponding metal chlorides;; | |
With hydrogen sulfide In neat (no solvent) byproducts: HCl; react. of dry H2S with PCl5 under heating;; | |
With hydrogen sulfide In neat (no solvent) byproducts: HCl; | |
With metal chloride In not given byproducts: metal sulfide; react. of PCl5 with metal chloride;; | |
With metal chloride In not given byproducts: metal sulfide; react. of PCl5 with metal chloride;; |
thiophosphoryl(V) bromide
phosphorus pentachloride
A
trichlorothiophosphine
B
phosphorus pentabromide
Conditions | Yield |
---|---|
In not given react. with PSBr3;; | |
In not given react. with PSBr3;; |
phosphorus pentachloride
hydrogen sulfide
trichlorothiophosphine
Conditions | Yield |
---|---|
In neat (no solvent) react. with liquid H2S;; | |
In carbon disulfide passing H2S through a liquid mixt. of PCl5 and CS2;; distn. in a stream of CO2;; | |
In not given react. of liquid H2S with PCl5;; |
phosphorus pentachloride
A
trichlorothiophosphine
Conditions | Yield |
---|---|
In neat (no solvent) react. on heating under blazing up;; |
phosphorus pentachloride
A
trichlorothiophosphine
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: thiosulfate; react. on haeting;; |
Conditions | Yield |
---|---|
In gas Kinetics; High Pressure; the reagent ions were generated in an electron impact high-pressure ion source contg. H2O; the reagent ions were selected using a quadrupole mass filter before being injected into a drift region contg. helium carriergas; at 298 K; monitoring by quadrupole mass spectrometer at the end of the flow tube; | A 100% B n/a |
Conditions | Yield |
---|---|
In gas Kinetics; High Pressure; the reagent ions were generated in an electron impact high-pressure ion source contg. H2O; the reagent ions were selected using a quadrupole mass filter before being injected into a drift region contg. helium carriergas; at 298 K; monitoring by quadrupole mass spectrometer at the end of the flow tube; | 100% |
Conditions | Yield |
---|---|
With caesium carbonate In acetonitrile at 0 - 20℃; for 12h; | 98% |
trichlorothiophosphine
chloro bis(3,5-bis(borane-diphenylphosphino)-phenoxy)thiophosphate
Conditions | Yield |
---|---|
In tetrahydrofuran byproducts: NaCl; in the absence of air using Schlenk techniques; mixed between -95 and -100°C under stirring; mixt. stirred overnight at room temp.; partially concd. (vac.); ppt. centrifuged; filtered under Ar; filtrate evapd; as oil; | 97.5% |
Conditions | Yield |
---|---|
In gas Kinetics; High Pressure; the reagent ions were generated in an electron impact high-pressure ion source contg. NO2; the reagent ions were selected using a quadrupole mass filter before being injected into a drift region contg. helium carriergas; at 298 K; monitoring by quadrupole mass spectrometer at the end of the flow tube; | A 97% B 3% C n/a D n/a |
trichlorothiophosphine
carbon monoxide
A
sulphur monochloride
B
PSCl2(1+)
D
PCl2(1+)
Conditions | Yield |
---|---|
In gas Kinetics; High Pressure; the reagent ions were generated in an electron impact high-pressure ion source contg. CO; the reagent ions were selected using a quadrupole massfilter before being injected into a drift region contg. helium carrier gas; at 298 K; monitoring by quadrupole mass spectrometer at the end of the flow tube; | A n/a B 93% C 1% D 6% E n/a |
trichlorothiophosphine
dinitrogen monoxide
A
sulphur monochloride
B
PSCl2(1+)
D
PCl2(1+)
Conditions | Yield |
---|---|
In gas Kinetics; High Pressure; the reagent ions were generated in an electron impact high-pressure ion source contg. N2O; the reagent ions were selected using a quadrupole mass filter before being injected into a drift region contg. helium carriergas; at 298 K; monitoring by quadrupole mass spectrometer at the end of the flow tube; | A n/a B 93% C 1% D 6% E n/a |
In gas Kinetics; byproducts: O; High Pressure; the reagent ions were generated in an electron impact high-pressure ion source contg. N2O; the reagent ions were selected using a quadrupole mass filter before being injected into a drift region contg. helium carriergas; at 298 K; O was also obtained; monitoring by quadrupole mass spectrometer at the end of the flow tube; | A n/a B 69% C 18% D 13% E n/a |
Conditions | Yield |
---|---|
In chloroform dissolving NH3-gas at -10°C in dry CHCl3; dropwisre addn. of PSCl3 in CHCl3 during 1.5 h; passing NH3 through the soln. at -10°C; sucking off; drying in vac. and dissolving in CHCl3; boiling for 3-4 h in presence of diethylamine;; recrystn. from hot methanol;; | 90% |
In chloroform dissolving NH3-gas at -10°C in dry CHCl3; dropwisre addn. of PSCl3 in CHCl3 during 1.5 h; passing NH3 through the soln. at -10°C; sucking off; drying in vac. and dissolving in CHCl3; boiling for 3-4 h in presence of diethylamine;; recrystn. from hot methanol;; | 90% |
In not given formation from PSCl3 and NH3;; |
trichlorothiophosphine
methylenebis(dichlorophosphine)
methylene-bis-(phosphonic dichloride)
Conditions | Yield |
---|---|
With aluminum (III) chloride at 110 - 140℃; for 6h; Inert atmosphere; | 89% |
trichlorothiophosphine
isopropyl alcohol
O-isopropyl phosphorodichloridothioate
Conditions | Yield |
---|---|
With pyridine at 20℃; for 2h; | 84% |
Conditions | Yield |
---|---|
Stage #1: para-tert-butylphenol With sodium hydroxide In water at 0℃; Stage #2: trichlorothiophosphine With tetrabutylammomium bromide In dichloromethane; water at 0 - 20℃; for 5h; | 81% |
Conditions | Yield |
---|---|
In gas Kinetics; byproducts: SCl, Cl2; High Pressure; the reagent ions were generated in an electron impact high-pressure ion source contg. N2; the reagent ions were selected using a quadrupole massfilter before being injected into a drift region contg. He; 298 K; SCl, Cl2 were also obtained; monitoring by quadrupole mass spectrometer at the end of the flow tube; | A 80% B 4% C 2% D 14% E n/a |
trichlorothiophosphine
carbon dioxide
A
sulphur monochloride
B
PSCl2(1+)
E
PCl2(1+)
Conditions | Yield |
---|---|
In gas Kinetics; byproducts: Cl, CCl; High Pressure; the reagent ions were generated in an electron impact high-pressure ion source contg. CO2; the reagent ions were selected using a quadrupole mass filter before being injected into a drift region contg. He; at 298 K; Cl, CCl were also obtained; monitoring by quadrupole mass spectrometer at the end of the flow tube; | A n/a B 80% C 11% D 3% E 6% |
Conditions | Yield |
---|---|
Stage #1: ortho-cresol With sodium hydroxide In water at 0℃; Stage #2: trichlorothiophosphine With tetrabutylammomium bromide In dichloromethane; water at 0 - 20℃; for 5h; | 80% |
Conditions | Yield |
---|---|
Stage #1: p-cresol With sodium hydroxide In water at 0℃; Stage #2: trichlorothiophosphine With tetrabutylammomium bromide In dichloromethane; water at 0 - 20℃; for 5h; | 76% |
Conditions | Yield |
---|---|
Stage #1: 2-fluorophenol With sodium hydroxide In water at 0℃; Stage #2: trichlorothiophosphine With tetrabutylammomium bromide In dichloromethane; water at 0 - 20℃; for 8h; | 75% |
Conditions | Yield |
---|---|
In gas Kinetics; High Pressure; the reagent ions were generated in an electron impact high-pressure ion source contg. O2/N2; the reagent ions were selected using a quadrupole mass filter before being injected into a drift region contg. helium carrier gas; at 298 K; monitoring by quadrupole mass spectrometer at the end of the flow tube; | A 21% B 73% C 6% D n/a |
trichlorothiophosphine
2-monochlorophenol
phosphorodichloridothioic acid O-ortho-chlorophenyl ester
Conditions | Yield |
---|---|
Stage #1: 2-monochlorophenol With sodium hydroxide In water at 0℃; Stage #2: trichlorothiophosphine With tetrabutylammomium bromide In dichloromethane; water at 0 - 20℃; for 8h; | 72% |
trichlorothiophosphine
carbon tetrafluoride
A
PSCl2(1+)
D
Cl3FP(1+)
Conditions | Yield |
---|---|
In gas Kinetics; byproducts: CF2, CF2S, CClF2; High Pressure; ions were generated in an electron impact high-pressure ion source contg. CF4; the reagent ions were selected using a quadrupole mass filter before being injected into a region contg. He; at 298 K; CF2, CF2S, CClF2, CFS, PS were obtained; monitoring by quadrupole mass spectrometer at the end of the flow tube; | A 4% B 2% C 69% D n/a E 25% |
trichlorothiophosphine
sulfur(VI) hexafluoride
A
ClS2(1+)
B
PSCl2(1+)
D
Cl3FP(1+)
Conditions | Yield |
---|---|
In gas Kinetics; byproducts: S2(1+), PFCl3, F; High Pressure; ions generated in an electron impact high-pressure ion source contg. SF6were selected using a quadrupole mass filter before being injected into a region contg. He; 298 K; S*PSCl3(1+), SF, SFCl, S2, ClF, ClP, FS2, S2 (1+), PFCl3, F were also obtained; monitoring by quadrupole mass spectrometer at the end of the flow tube; | A 4% B 14% C 69% D 6% E 3% |
trichlorothiophosphine
sulfur(VI) hexafluoride
A
FS2(1+)
D
Cl3FP(1+)
Conditions | Yield |
---|---|
In gas Kinetics; byproducts: SF2, F2, PFCl3; High Pressure; the ions were generated in an electron impact high-pressure ion source contg. SF6; the ions were selected using a quadrupole mass filter before being injected into a drift region contg. He carrier gas; 298 K; SF2, F2, PFCl3, FS2, SSF2 were also obtained; monitoring by quadrupole mass spectrometer at the end of the flow tube;; | A 8% B 66% C 13% D 8% E 5% |
Conditions | Yield |
---|---|
In water at 3 - 95℃; for 2.66667h; Product distribution / selectivity; Heating / reflux; | 65% |
trichlorothiophosphine
carbon tetrafluoride
B
SCF(1+)
C
PCl2(1+)
D
PS(1+)
E
fluorodichloromethyl(1+)
Conditions | Yield |
---|---|
In gas Kinetics; byproducts: CFSCl3(1+), PFCl3(1+), CClS(1+); High Pressure; ions generated in an electron impact high-pressure source contg. CF4 were selected using a mass filter before being injected into a region contg. He; 298 K; CFSCl3(1+), PFCl3(1+), CClS(1+), CCl3F, PCl3, CClS, CClFS, PSCl, P, CS, PFCl2 were also obtained; monitoring by quadrupole mass spectrometer at the end of the flow tube; | A 15% B 64% C n/a D n/a E 9% |
Conditions | Yield |
---|---|
In gas Kinetics; byproducts: Cl, N, PS(1+); High Pressure; ions generated in an electron impact high-pressure source contg. N2 wereselected using a quadrupole mass filter before being injected into a dr ift region contg. He; at 298 K; PS(1+), Cl, N, SCl, PCl3, Cl2, NCl3 werealso obtained; monitoring by quadrupole mass spectrometer at the end of the flow tube; | A 62% B 1% C 16% D 15% E 5% |
trichlorothiophosphine
ammonium chloride
dichlorothiophosphoric acid amide
Conditions | Yield |
---|---|
for 20h; Reflux; | 58.5% |
Conditions | Yield |
---|---|
In water for 0.5h; Product distribution / selectivity; Reflux; | 56.5% |
In water according to S.K. Yasuda, J.L. Lambert, Inorg. Synth. 1957, 5, 102; PSCl3 added to aq. NaOH; suspended in anhydr. methanol; | 42% |
In neat (no solvent) | |
In neat (no solvent) | |
In water react. of aq. NaOH and PSCl3; |
trichlorothiophosphine
A
diferrocenyl chlorothiophosphonate
Conditions | Yield |
---|---|
With NEt3 In tetrahydrofuran byproducts: NEt3HCl; Ar-atmosphere; mixing equimolar amt. of ferrocene derivative and NEt3, cooling to -78°C, slow addn. of 0.5 equiv. of PSCl3, stirring (room temp., overnight); filtration, evapn. (vac.), chromy. (SiO2, CH2Cl2); | A 49% B n/a |
trichlorothiophosphine
carbon tetrafluoride
A
PSCl2(1+)
C
Cl3FP(1+)
D
thiocarbonyl fluoride
E
chlorotrifluoromethane
Conditions | Yield |
---|---|
In gas Kinetics; High Pressure; the reagent ions were generated in an electron impact high-pressure ion source contg. CF4; the reagent ions were selected using a quadrupole mass filter before being injected into a drift region contg. helium carriergas; at 298 K; monitoring by quadrupole mass spectrometer at the end of the flow tube; | A 48% B 44% C 8% D n/a E n/a |
trichlorothiophosphine
dinitrogen monoxide
A
PSCl2(1+)
D
PCl2(1+)
E
nitrogen(II) oxide
Conditions | Yield |
---|---|
In gas Kinetics; byproducts: ClNOS, ClNO; High Pressure; the reagent ions were generated in an electron impact high-pressure ion source contg. N2O; the reagent ions were selected using a quadrupole mass filter before being injected into a region contg. He; at 298 K; ClNO, ClNOS were also obtained; monitoring by quadrupole mass spectrometer at the end of the flow tube; | A 7% B 47% C 33% D 13% E n/a |
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