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2351-34-0

2351-34-0 Structure

2351-34-0 Structure
IdentificationBack Directory
[Name]

1-CHLORO-1-METHYLSILACYCLOBUTANE
[CAS]

2351-34-0
[Synonyms]

1-Chloro-1-methylsiletane
1-CHLORO-1-METHYLSILACYCLOBUTANE
Silacyclobutane, 1-chloro-1-methyl-
CYCLOTRIMETHYLENEMETHYLCHLOROSILANE
1-Chloro-1-Methylsilacyclobutane 98%
[Molecular Formula]

C4H9ClSi
[MDL Number]

MFCD00191926
[MOL File]

2351-34-0.mol
[Molecular Weight]

120.65
Chemical PropertiesBack Directory
[Boiling point ]

103 °C(lit.)
[density ]

0.985 g/mL at 25 °C(lit.)
[refractive index ]

n20/D 1.45(lit.)
[Fp ]

37 °F
[solubility ]

soluble in most aprotic organic solvents.
[form ]

liquid
[Specific Gravity]

0.985
[Hydrolytic Sensitivity]

8: reacts rapidly with moisture, water, protic solvents
[InChI]

InChI=1S/C4H9ClSi/c1-6(5)3-2-4-6/h2-4H2,1H3
[InChIKey]

JWKKXHBGWAQZOK-UHFFFAOYSA-N
[SMILES]

[Si]1(Cl)(C)CCC1
Safety DataBack Directory
[Hazard Codes ]

F,C
[Risk Statements ]

11-14-34
[Safety Statements ]

16-26-36/37/39-45
[RIDADR ]

UN 2985 3/PG 2
[WGK Germany ]

3
[TSCA ]

No
[Storage Class]

3 - Flammable liquids
[Hazard Classifications]

Flam. Liq. 2
Skin Corr. 1B
Hazard InformationBack Directory
[Physical properties]

bp 103°C; d 0.985 g cm?3.
[Uses]

Intermediate in the formation of enoxysilacyclobutanes.
[Uses]

Siletanes (silacyclobutanes) represent a unique class of silicon-based reagents that have enjoyed much success in a number of synthetic applications including aldol reactions, allylations, cross-coupling reactions, carbosilane oxidations, and ring expansions. The manifestation of their strain in enhanced Lewis acidity and in the ring opening to silanols accounts for their utility. 1-Chloro-1-methylsiletane can be used for the preparation of the various siletane derivatives for these applications.
Grignard reagents react efficiently with 1-chloro-1-methylsiletane to provide the corresponding aryl-, alkenyl-, or alkylsiletanes (eqs 1–3).On the contrary, reactions with alkyllithiums are limited to the reaction of 1 with a lithium acetylide (eq 4).The reaction of 1 with an intermediate vinylalane obtained by hydroalumination of 1-heptyne gave (E)-1-heptenylmethylsiletane in >99/1 isomeric purity (eq 5).The reaction of 1 with LiAlD4 afforded 1-deuterio-1-methylsiletane (eq 6).

[Preparation]

siletane can be prepared in large quantities byWurtz coupling reaction of dichloro-3-chloropropylmethylsilane with Mg.It is commercially available from Gelest and Aldrich chemical company.
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