335452
Lithium (trimethylsilyl)acetylide solution
0.5 M in THF
Synonym(s):
(Trimethylsilyl)ethynyllithium
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About This Item
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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 Statements
Precautionary Statements
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
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Lithium (Trimethylsilyl) acetylide
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
Tetrahedron, 62(26), 6312-6320 (2006)
Chemistry of Materials, 6, 636-636 (1994)
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