ETHYNYL P-TOLYL SULFONE Chemical Properties

Melting point:

73-74 °C (lit.)

Boiling point:

297.9±33.0 °C(Predicted)

Density 

1.219±0.06 g/cm3(Predicted)

storage temp. 

Inert atmosphere,Room Temperature

solubility 

organic solvents: soluble(lit.)

form 

powder to crystal

color 

White to Light yellow

BRN 

2556169

Safety Information

Hazard Codes 

Xi

Risk Statements 

36/37/38

Safety Statements 

26-36

WGK Germany 

3

HS Code 

29041000

MSDS

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ETHYNYL P-TOLYL SULFONE Usage And Synthesis

Uses

Ethynyl p-tolyl sulfone (Tosylacetylene) may be used in the synthesis of 2-(4-methylphenylsulfonyl)ethenyl (tosvinyl, Tsv) protected derivatives. It may be used as starting reagent for the synthesis of optically active indan-2-ols.

Application

Ethynyl p-Tolyl Sulfone is a dienophile used in electrocyclic reactions such as dipolar cycloaddition, Diels-Alder reaction, and ene cyclization; electron-poor Michael acceptor in conjugate additions; undergoes direct displacement with organometallic complexes to give aryl- or alkylacetylenes.

Preparation

Ethynyl p-Tolyl Sulfone has been prepared by several groups over the years employing a variety of synthetic strategies including ethynyl Grignard addition to p-toluenesulfonyl fluoride, dehydroiodination of (E)-2-iodo-1- tosyl-1-ethene, oxidative elimination of β-[(4-methylphenyl)seleno]vinyl sulfone, dehydrobromination of cis-and trans-2-bromovinyl 4-methylphenyl sulfone,23 diazotization of 4-[(4-methylphenyl)sulfonyl]-5- aminoisoxazole, and oxidation of ethynyl thioether. The modified strategy commonly used today is an established Friedel-Crafts based procedure first performed by Bhattacharya et al. but recently exploited by Waykole and Paquette (eq 1). Its simplicity and mildness has shown it to be broadly useful since it bypasses the need for immoderate conditions encountered in the earlier strategies.

Synthesis Reference(s)

The Journal of Organic Chemistry, 57, p. 697, 1992 DOI: 10.1021/jo00028a053

storage

Decomposition of the intermediate complex p-toluenesulfonyl chloride-aluminum chloride-bis(trimethylsilyl)acetylene with hydrochloric acid and ice is exothermic and due caution is recommended. Also, a nitrogen atmosphere is suggested throughout its preparation due to the hygroscopic nature of the reagents and intermediate(s) involved.

Purification Methods

Recrystallise the sulfone from pet ether, *C6H6 or EtOH (m 66o), and dry it in a vacuum. [Beilstein 6 III 1397, 6 IV 2160.]

ETHYNYL P-TOLYL SULFONE(13894-21-8)Related Product Information

• Phenylthioacetylene
• Ethyl 4-acetyl tetrahydro-2H-pyran-4-carboxylate
• DI-TERT-BUTYL ACETYLENEDICARBOXYLATE
• 2-(TRIMETHYLSILYL)ETHYNYL P-TOLYL SULFONE
• 1-(p-Toluenesulfonyl)-2-(trimethylsilyl)acetylene, 2-(Trimethylsilyl)ethynyl p-tolyl sulfone
• ETHYNYL P-TOLYL SULFONE