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Sigma-Aldrich

Lithium (trimethylsilyl)acetylide solution

0.5 M in THF

Synonym(s):

(Trimethylsilyl)ethynyllithium

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About This Item

Linear Formula:
(CH3)3SiC≡CLi
CAS Number:
Molecular Weight:
104.15
Beilstein:
3587411
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22

form

liquid

Quality Level

concentration

0.5 M in THF

density

0.88 g/mL at 25 °C

SMILES string

[Li]C#C[Si](C)(C)C

InChI

1S/C5H9Si.Li/c1-5-6(2,3)4;/h2-4H3;

InChI key

ZVXXEONXFWSCIZ-UHFFFAOYSA-N

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Application

Lithium (trimethylsilyl)acetylide can be used as a reagent:
  • In the transmetalation and nucleophilic displacement reactions.
  • To prepare propargylic alcohol derivatives by reacting with aldehydes and ketones.
  • To synthesize α,βynones by treating with Weinreb amide or with isoxazolidide.
  • Along with Grignard reagent to convert γ- and δ-thiolactams to thioiminium salts, which are employed as key intermediates to produce disubstituted pyrrolidines.

Reacts with halotriazines to produce conductive, anisotropic carbon-nitrogen materials.

Packaging

The 25 mL Sure/Seal bottle is recommended as a single-use bottle. Repeated punctures will likely result in decreased performance of product.

Legal Information

Sure/Seal is a trademark of Sigma-Aldrich Co. LLC

Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Oral - Carc. 2 - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B - STOT SE 3

Target Organs

Respiratory system

Supplementary Hazards

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

-9.4 °F - closed cup

Flash Point(C)

-23 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Lithium (Trimethylsilyl) acetylide
Fuhry MM
Encyclopedia of Reagents for Organic Synthesis, Second Edition (2001)
Sequential addition reaction of lithium acetylides and Grignard reagents to thioiminium salts from thiolactams leading to 2, 2-disubstituted cyclic amines
M Toshiaki, et al.
Tetrahedron, 62(26), 6312-6320 (2006)
Chemistry of Materials, 6, 636-636 (1994)

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