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Thiocarbonyl dichloride

Methyl 3-chloroformyl-2-pyrazinecarboxylate (129) gave methyl 3-carbamoyl-2-pyrazinecarboxylate (130) [HN(SiMe3)2, CHC13, 0°C —> reflux, 90 min then residue from evaporation, H20, reflux, 30 min 75%. Note survival of the ester grouping under these conditions].1185 l,4-Piperazinedi(thiocarbonyl) dichloride (131) gave l,4-bis[morpholino(thio-formyl)]piperazine (132) [neat 0(CH2CH2)NH, warmed briefly >95%].350... [Pg.319]

PROP Reddish, fuming, red liquid with acrid odor. Bp 73.5°, d 1.5085 15°. Decomp in water and ale. Sltly sol in H2O sol in Et20. Slowly hydrolyzes by H2O. SYNS CARBON CHLOROSULFIDE CARBONO-THIOIC DICHLORIDE (9CI) CARBONYL CHLORIDE, THIO- DICHLOROTHIOCARBONYL PHOSGENE, THIO- THIOCARBONIC DICHLORIDE THIO-CARBONYL CHLORIDE THIOCARBONYL DICHLORIDE THIOFOSGEN (CZECH) THIO-KARBONYLCHLORID (CZECH)... [Pg.1337]

Bis(trimethylsilyl)piperazine (123) gave l,4-piperazinedi(thiocarbonyl) dichloride (124) (CSCb, CCI4, -23 20°C >95%) ... [Pg.318]

Piperazinedi(thiocarbonyl) dichloride (131) gave l,4-bis[morpholino(thio-formyl)]piperazine (132) [neat O(( tl,( tt,)NH, warmed briefly >95%]. °... [Pg.319]

THIOCARBONYL DICHLORIDE (463-71-8) Reacts with water, decomposing to hydrochloric acid and sulfur dioxide, carbon disulfide, and carbon dioxide. Aqueous solution is incompatible with sulfuric acid, alkalis, ammonia, aliphatic amines, alkanolamines, alkylene oxides, amides, epichlorohydrin, organic anhydrides, isocyanates, vinyl acetate. Corrodes most metals in the presence of moisture. [Pg.1145]

Thiocarbanilide. See N,N -Diphenylthiourea Thiocarbonic dichloride Thiocarbonyl chloride Thiocarbonyl dichloride. See Thiophosgene Thiocarbonyl tetrachloride. See Perchloromethyl mercaptan Thiochroman-4-one. See Thallium (I) carbonate 4-Thiocresol. See p-Thiocresol o-Thiocresol CAS 137-06-4... [Pg.4411]

Titanium tetrachloride Thiocarbonyl dichloride Thionyl fluoride Thiophosgene Triethyl aluminum Trifluoromethyl iodide Tiiisohutylaluminum Trimethylaluminum Vanadium tetrachloride Vincennite Vinyl hromide Vinyhnagnesium bromide Xenon difluoride Zinc arsenide... [Pg.66]

Alkylaminocarbonyl- -dialkylester XII/2, 43 Alkvlamino-thiocarbonyl- -dialkylester XII/2, 43 aus Phosphorigsaure-dialkylester und Isothio-cyanat allgemeine Arbeitsweise XII/1, 458 Alkylthio-carbonyl- -dialkylester XII/2, 43 Alkylthio-cthin- -dialkylester E2, 373 Alkylthio-thiocarbonyl- -dialkylester XII/2, 43 Allen- -dichlorid E2, 326... [Pg.1026]

Olefinations. Reaction of carbonyl compounds with gem-dichlorides in the presence of Zn-MCjSiCl provides alkenes. Reformatsky reaction on thiocarbonyl compounds also gives conjugated esters. [Pg.436]

Bis(thiocarbonyl)hydrazide derivatives of galactaric acid (186,187) have been prepared by reaction of 2,3,4,5-tetra-Oacetyl-D-galactaroyl dichloride (185) with 4-arylthiosemicarbazides335 or S-methyl(benzyl) hy-drazinecarbodithioates336 (Scheme 56). The adducts were subsequently converted into a variety of bis(heterocyclic) compounds including thiadia-zole, triazole, and oxadiazole derivatives. The tetraacetates 186 have been... [Pg.99]

A complex reaction of 4-methylquinoline (187) with thionyl chloride gives a [l,2]dithiolo[3,4-c]quinolin-l-one (189) [88JCS(Pl)3025j initial formation of the thiocarbonyl chloride (188) was proposed, as shown in Scheme 43, and susequent steps probably involved disulfur dichloride formed in situ. [Pg.208]


See other pages where Thiocarbonyl dichloride is mentioned: [Pg.183]    [Pg.846]    [Pg.1908]    [Pg.1003]    [Pg.250]    [Pg.60]    [Pg.61]    [Pg.218]    [Pg.10]    [Pg.429]    [Pg.183]    [Pg.846]    [Pg.1908]    [Pg.1003]    [Pg.250]    [Pg.60]    [Pg.61]    [Pg.218]    [Pg.10]    [Pg.429]    [Pg.36]    [Pg.153]    [Pg.36]    [Pg.36]    [Pg.1360]    [Pg.128]    [Pg.54]    [Pg.36]    [Pg.618]    [Pg.275]   


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