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761060

Sigma-Aldrich

(Tributylphosphoranylidene)acetonitrile

97%

Synonym(s):

(Cyanomethylene)tributylphosphorane

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$237.00

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Estimated to ship onMarch 29, 2025

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1 G
$237.00

About This Item

Empirical Formula (Hill Notation):
C14H28NP
CAS Number:
157141-27-0
Molecular Weight:
241.35
MDL number:
MFCD01321151
UNSPSC Code:
12352000
NACRES:
NA.22
form:
liquid
assay:
97%

$237.00

Estimated to ship onMarch 29, 2025

Request a Bulk Order

Quality Level

100

assay

97%

form

liquid

refractive index

n20/D 1.500 (lit.)

density

0.921 g/mL at 25 °C

storage temp.

2-8°C

SMILES string

[P](=CC#N)(CCCC)(CCCC)CCCC

InChI

1S/C14H28NP/c1-4-7-11-16(14-10-15,12-8-5-2)13-9-6-3/h14H,4-9,11-13H2,1-3H3

InChI key

OZMLUMPWPFZWTP-UHFFFAOYSA-N

General description

(Tributylphosphoranylidene)acetonitrile or cyanomethylenetrimethylphosphorane (Bu3P=CHCN) is a Wittig reagent employed in the transformation of the carbonyl compounds, including aldehydes, esters, and lactones into the corresponding unsaturated nitriles.[1]

Application

(Tributylphosphoranylidene)acetonitrile can be utilized as a reagent in the:
  • Stereoselective synthesis of skytanthine and other O- and N-containing heterocycles by Mitsunobu intramolecular cycloalkylation.[2]
  • Wittig olefination of esters, lactones, N-Boc lactam, and cyclic imide to corresponding Wittig products.[3]

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
MKCL5715
MKCL4453
MKCD4647
MKCB8261
MKBK3789

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Formation of heterocycles by the Mitsunobu reaction. Stereoselective synthesis of (+)-α-skytanthine
Tsunoda T, et al.
Tetrahedron Letters, 37(14), 2463-2466 (1996)
(Tributylphosphoranylidene) acetonitrile
Wyatt, Peter B
Encyclopedia of Reagents for Organic Synthesis, Second Edition (2001)
Cyanomethylenetrimethylphosphorane, a powerful reagent for the Wittig olefination of esters, lactones and imides
Tsunoda T, et al.
Tetrahedron Letters, 41(2), 235-237 (2000)

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