Chemistry:Triphenylcarbethoxymethylenephosphorane
From HandWiki
| |||
Names | |||
---|---|---|---|
Preferred IUPAC name
Ethyl (triphenyl-λ5-phosphanylidene)acetate | |||
Other names
(2-Ethoxy-2-oxoethylidene)triphenylphosphorane
(Carbethoxymethylene)triphenylphosphorane | |||
Identifiers | |||
3D model (JSmol)
|
|||
ChemSpider | |||
PubChem CID
|
|||
UNII | |||
| |||
| |||
Properties | |||
C22H21O2P | |||
Molar mass | 348.382 g·mol−1 | ||
Melting point | 124 to 129 °C (255 to 264 °F; 397 to 402 K) | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |||
Infobox references | |||
Tracking categories (test):
Triphenylcarbethoxymethylenephosphorane is an organophosphorus compound with the chemical formula Ph3PCHCO2Et (Ph = phenyl, Et = ethyl). It is a white solid that is soluble in organic solvents.
The compound is a Wittig reagent. It is used to replace oxygen centres in ketones and aldehydes with CHCO2Et.[1]
References
- ↑ Lang, R. W.; Hansen, H.-J. (1984). "α-Allenic Esters from α-Phosphoranylidene Esters and Acid Chlorides: Ethyl 2,3-Pentadienoate". Organic Syntheses 62: 202. http://www.orgsyn.org/orgsyn/pdfs/CV7P0232.pdf.; Collective Volume, 7, pp. 232
Original source: https://en.wikipedia.org/wiki/Triphenylcarbethoxymethylenephosphorane.
Read more |