ChemicalBook Product Catalog Organic Chemistry Phosphines (FORMYLMETHYLENE)TRIPHENYLPHOSPHORANE

(FORMYLMETHYLENE)TRIPHENYLPHOSPHORANE

(FORMYLMETHYLENE)TRIPHENYLPHOSPHORANE Basic information
Product Name:(FORMYLMETHYLENE)TRIPHENYLPHOSPHORANE
Synonyms:(Formylmethylene)triphenylphosphorane, 97%, may cont. up to ca 3% water;FORMYLMETHYLENETRIPHENYLPHOSPORANE;Formylmethylenetriphenylphosphorane, 98 %;2-Oxoethylidenetriphenylphosphorane;Triphenyl(2-oxoethylidene)phosphorane;(Triphenylphosphoranylidene)acetaldehyde,97%;(Triphenylphosphoranylidene)acetaldehydeDISC 10/19/00;Acetaldehyde, 2-(triphenylphosphoranylidene)-
CAS:2136-75-6
MF:C20H17OP
MW:304.32
EINECS:218-375-6
Product Categories:Wittig Reagents;Synthetic Organic Chemistry;Wittig & Horner-Emmons Reaction;Wittig Reaction
Mol File:2136-75-6.mol
(FORMYLMETHYLENE)TRIPHENYLPHOSPHORANE Structure
(FORMYLMETHYLENE)TRIPHENYLPHOSPHORANE Chemical Properties
Melting point 185-188 °C(lit.)
Boiling point 472.6±28.0 °C(Predicted)
density 1.16±0.1 g/cm3(Predicted)
storage temp. Inert atmosphere,Store in freezer, under -20°C
solubility Soluble in Chloroform, Methanol.
form Fine Crystalline Powder
color Pink to brown
Sensitive Air Sensitive
BRN 523797
Stability:Stable. Combustible. Incompatible with strong oxidizing agents.
InChIKeyCQCAYWAIRTVXIY-UHFFFAOYSA-N
CAS DataBase Reference2136-75-6(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 3
Hazard Note Irritant/Keep Cold/Air Sensitive
HS Code 29319090
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
ALFA English
(FORMYLMETHYLENE)TRIPHENYLPHOSPHORANE Usage And Synthesis
Chemical Propertiespink to brown crystalline powder
UsesWittig reagent for the conversion of aldehydes and ketones to two-carbon homologated, α,β-unsaturated carbonyl compounds.
Uses(Formylmethylene)triphenylphosphorane is used as Wittig reagent. It is also used as Pharmaceutical Intermediates. It is employed as raw material in organic Synthesis, Agrochemicals.
Purification MethodsRecrystallise it from Me2CO, or dissolve it in *C6H6, wash with N NaOH, dry (MgSO4), evaporate, and crystallise the residue from Me2CO. It can be prepared from its precursor, formylmethyltriphenylphosphonium chloride (which crystallises from CHCl3/EtOAc), by treatment with Et3N and extraction with *C6H6. [Tripett & Walker J Chem Soc 1266 1961.]
(FORMYLMETHYLENE)TRIPHENYLPHOSPHORANE Preparation Products And Raw materials
Preparation Products(3S,4R)-4-Acetoxy-3-[(R)-1-(tert-butyldimethylsilyloxy)ethyl]azetidin-2-one-->Diphenylacetylene-->VINYLCYCLOHEXANE-->3,5-BIS(BENZYLOXY)BENZYL BROMIDE-->3-NAPHTHALEN-2-YL-PROPIONALDEHYDE-->Cefdinir-->3-（trifluoromethyl) Cinnamaldehyde-->5-Nitrofuran-2-acrylaldehyde-->FENPICLONIL-->2-Propenal, 3-(2-thiazolyl)-, (2E)--->2-Propenal, 3-(3,5-difluorophenyl)-, (2E)--->(2E,2'E)-3,3'-(1,4-phenylene)diacrylaldehyde
DIPHENYL(P-TOLYL)PHOSPHINE BIS(TRIPHENYLPHOSPHINE)DICARBONYLNICKEL TRIPHENYLPHOSPHINE DIBROMIDE TRIPHENYLPHOSPHINE SULFIDE TRIS(3-METHOXYPHENYL)PHOSPHINE [3-(Dimethylamino)propyl]triphenylphosphonium bromide hydrobromide DICHLORODICARBONYLBIS(TRIPHENYLPHOSPHINE)RUTHENIUM (II) TRI-P-TOLYLPHOSPHINE P-ANISYLDIPHENYLPHOSPHINE Ethyl (triphenylphosphoranylidene)acetate BIS(TRIPHENYLPHOSPHINE)COBALT (II) CHLORIDE DIPHENYL(O-TOLYL)PHOSPHINE Ethyl 2-(triphenylphosphoranylidene)propionate (4-bromophenyl)diphenylphosphine Bis(triphenylphosphine)nickel(II)chloride (CYCLOPENTADIENYLIDENE)TRIPHENYLPHOSPHORANE Bis(triphenylphosphine)palladium(II) chloride 2-(TRIPHENYLPHOSPHORANYLIDENE)SUCCINIC ANHYDRIDE
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