ChemicalBook >> CAS DataBase List >>ETHYNYL P-TOLYL SULFONE

ETHYNYL P-TOLYL SULFONE

CAS No.
13894-21-8
Chemical Name:
ETHYNYL P-TOLYL SULFONE
Synonyms
1-(ethynylsulfonyl)-4-Methylbenzene;TOSYLACETYLENE;ETHYNYL P-TOLYL SULFONE;Ethynylp-TolylSulfone>p-tolylsulfonylacetylene;4-(Ethynylsulfonyl)toluene;P-TOLUENESULFONYLACETYLENE;Ethynyl p-Tolyl Sulfone;Benzene, 1-(ethynylsulfonyl)-4-methyl-;p-Toluenesulfonylacetylene, Tosylacetylene
CBNumber:
CB3427572
Molecular Formula:
C9H8O2S
Molecular Weight:
180.22
MDL Number:
MFCD00191647
MOL File:
13894-21-8.mol
MSDS File:
SDS
Last updated:2025-07-14 15:27:00

ETHYNYL P-TOLYL SULFONE 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
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P264-P271-P280-P302+P352-P305+P351+P338
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36
WGK Germany  3
HS Code  29041000
NFPA 704
0
2 0

ETHYNYL P-TOLYL SULFONE price More Price(15)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 419869 Ethynyl p-tolyl sulfone 98% 13894-21-8 1g $113 2025-07-31 Buy
TCI Chemical E0466 Ethynyl p-Tolyl Sulfone >98.0%(GC) 13894-21-8 1g $201 2025-07-31 Buy
TCI Chemical E0466 Ethynyl p-Tolyl Sulfone >98.0%(GC) 13894-21-8 5g $638 2025-07-31 Buy
TRC E938863 Ethynyl p-Tolyl Sulfone 13894-21-8 50mg $45 2021-12-16 Buy
AK Scientific 7929AL Ethynyl p-Tolyl Sulfone 13894-21-8 5g $343 2021-12-16 Buy
Product number Packaging Price Buy
419869 1g $113 Buy
E0466 1g $201 Buy
E0466 5g $638 Buy
E938863 50mg $45 Buy
7929AL 5g $343 Buy

ETHYNYL P-TOLYL SULFONE Chemical Properties,Uses,Production

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.
ETHYNYL P-TOLYL SULFONE synthesis

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 Preparation Products And Raw materials

Global( 99)Suppliers
Supplier Tel Email Country ProdList Advantage
Frapp's ChemicalNFTZ Co., Ltd.
+86 (576) 8169-6106 sales@frappschem.com China 880 50
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 33024 60
Jinan Carbotang Biotech Co.,Ltd.
+8615866703830 figo.gao@foxmail.com China 8497 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 49733 58
Shanghai Safer Pharmaceutical Technology Co., Ltd.
021-31761238 sales@saferph.com CHINA 897 58
Neostar United (Changzhou) Industrial Co., Ltd.
+86-0519-85551759 +8613506123987 marketing1@neostarunited.com China 8829 58
Dayang Chem (Hangzhou) Co.,Ltd.
+86-0571-88938639 +8617705817739 info@dycnchem.com China 52846 58
CD Chemical Group Limited
+8615986615575 info@codchem.com China 20342 58
GLR Innovations
+91 9891111994 info@glrgroup.in India 4535 58
Hebei Chuanghai Biotechnology Co., Ltd
+8615531151365 mina@chuanghaibio.com China 18126 58
Ethynyl p-Tolyl Sulfone ETHYNYL P-TOLYL SULFONE P-TOLUENESULFONYLACETYLENE TOSYLACETYLENE p-Toluenesulfonylacetylene, Tosylacetylene p-tolylsulfonylacetylene Ethynylp-TolylSulfone> 4-(Ethynylsulfonyl)toluene Benzene, 1-(ethynylsulfonyl)-4-methyl- 1-(ethynylsulfonyl)-4-Methylbenzene 13894-21-8 CH3C6H4SO2C8801CH C9H8O2S Sulfur Compounds Sulfones Organic Building Blocks Acetylenes Sulfur Compounds (for Synthesis) Functionalized Acetylenes Building Blocks Acetylenes Functionalized Acetylenes Sulfur Compounds (for Synthesis) Synthetic Organic Chemistry