トリメチルシリルアセチレン

Trimethylsilylacetylene

HCID 66111CAS 1066-54-2

基本情報

標準SMILES
C#C[Si](C)(C)C
InChIKey
CWMFRHBXRUITQE-UHFFFAOYSA-N
分子式
C5H10Si
平均分子量
98.22 g/mol
単同位体質量
98.05517685

名称と識別子

優先名称
Trimethylsilylacetylene
IUPAC
ethynyl(trimethyl)silane
現地名
トリメチルシリルアセチレン
英語名
Trimethylsilylacetylene
分子式
C5H10Si
分子量
98.22

名称と別名

EthynyltrimethylsilaneTrimethylsilylacetylene1066-54-2(Trimethylsilyl)acetyleneethynyl(trimethyl)silaneethynyl-trimethyl-silaneSilane, ethynyltrimethyl-trimethylsilyl acetylenetrimethylsilylethyne(Trimethylsilyl)ethyneTMS acetyleneTMS-acetylene
名称をさらに表示
トリメチルシリルアセチレン1-トリメチルシリルエチン1-(トリメチルシリル)エチン(トリメチルシリル)エチントリメチルエチニルシランエチニルトリメチルシラントリメチルシリルエチントリメチル(エチニル)シラン(トリメチルシリル)アセチレン1-(トリメチルシリル)アセチレンTMSアセチレンTMSAETHINYLTRIMETHYLSILANE1-TrimethylsilylethyneThimethylsilylacetylene(Thrimethylsilyl)acetylene
C5H10SiMFCD00008569(Trimethylsilyl)acetylene-dTrimethylethynylsilaneethynyltrimethyl silanetrimethylsilyl-acetylene1-(Trimethylsilyl)acetylenetms-acetylide

データベース識別子

CAS
1066-54-2、7299-46-9
PubChem CID
66111
DTXSID
DTXSID7061435
EC Number
213-919-9、685-813-4
Nikkaji
J209.060K

物性

構造計算による物性

極性表面積
0 Ų
水素結合供与体数
0
水素結合受容体数
0
回転可能結合数
1
重原子数
6

実験および物理化学的性質

Chemical ClassesMetals -> Metalloid Compounds (Silicon)
SpringerMaterials Properties29Si nuclear magnetic resonance spectrum
Vapor Pressure224.0 [mmHg]
Physical DescriptionColorless liquid; [Alfa Aesar MSDS]

物理化学的性質

融点
0 °C · >0°C
沸点
53 °C · 53 °C(lit.)
比重(密度)
0.695 g/mL · 0.695 g/mL at 25 °C(lit.)
蒸気圧
4.18 psi · 4.18 psi ( 20 °C)
屈折率
20 · n20/D 1.388(lit.)
闪点
30 °F · <−30 °F

化学的性質

化学的特性CLEAR COLORLESS LIQUID

安全と法規制

GHS分類

GHS Classification · 6 件

Danger

H225 (72.1%): Highly Flammable liquid and vapor [Danger Flammable liquids]

P210, P233, P240, P241, P242, P243, P261, P264, P264+P265, P271, P280, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P305+P354+P338, P317, P319, P321, P332+P317, P337+P317, P362+P364, P370+P378, P403+P233, P403+P235, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 86 reports by companies from 12 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Danger

H225 (100%): Highly Flammable liquid and vapor [Danger Flammable liquids]

危険有害性情報

Regulatory Information · 2 件

Status: Active Update: 02-06-2022 https://echa.europa.eu/registration-dossier/-/registered-dossier/33552

Trimethylsilylacetylene: HSNO Approval: HSR006727 Approved with controls

Hazards SummaryMay cause irritation; [Alfa Aesar MSDS] See 1-Phenyl-2-(trimethylsilyl)acetylene and Phenylacetylene.
Hazard Classes and Categories · 2 件

Flam. Liq. 2 (72.1%)

Flam. Liq. 2 (100%)

CSL Reaction Information · 6 件

CSL00196

(Trimethylsilyl)acetylene + Acetone + Oxygen

"We would like to report an explosion that occurred in our laboratory last year while performing an oxidative coupling of trimethylsilylacetylene (TMSA) in a Glaser-Hay reaction. The explosion ruptured the 2-L reaction flask and seriously injured a researcher. This reaction has been routinely used in our and many other laboratories to prepare 1,4-bis(trimethylsilyl)butadiyne-1,3 on a large scale (>100 g), and no dangerous or unusual behavior was previously noted. The procedure involves purging oxygen through a solution of TMSA in acetone in the presence of a copper(I) chloride:tetramethylethylenediamine complex catalyst at room temperature as described by Andrew B. Holmes et al. (Org. Syntheses 1993, Coll. Vol. 8, 63). The authors of the procedure recommend a safety shield as a general precaution while working with flammable materials in the atmosphere of oxygen, although no hazard was ever encountered. In this incident, the explosion occurred as soon as we started adding the solution of catalyst in acetone to the reaction. We have consulted with the pioneer of this reaction (Allan S. Hay) and the submitting author of the procedure (Holmes) and considered various scenarios to explain the explosion. Ignition of acetone/TMSA vapor by the external sources was hardly possible as the flask was well sealed and the outgoing gases were passed through a dry-ice condenser (lowering the vapor pressure below the explosive concentration) and brought to the back side of the fume hood through a 1-meter hose. The reaction temperature (5 ºC) was noted by the researcher a few seconds before the explosion, thus ruling out unexpected reaction exothermy. The autoignition of the vapor on a hot stirring adapter (possibly heated by rotation-induced friction) was refuted, because joint lubrication was checked before setting up the experiment, and it would have required achieving an unrealistic temperature of greater than 300 ºC. Also, the explosion occurred upon adding the first few drops of copper catalyst, which makes crystallization of the explosive intermediate—copper bis(trimethylsilylacetylide)—highly improbable. We speculate that a discharge of static electricity between the syringe needle and the digital thermometer inside the flask is the most likely cause of this explosion. A digital thermometer connected to a stirring hot plate (IKA) was used in the reaction, and a plastic syringe with a long metal needle was introduced through the same neck. An induced static voltage on the syringe through friction from handling (often observed in Montreal winter indoors while walking or even simply sitting) could then cause a sufficient differential potential on the needle for a discharge spark to occur close to the metallic body of the digital thermometer. The oxygen-rich atmosphere lowers the ignition energy and makes even a weak spark sufficient to cause a fire. The incident emphasizes once more the potential danger of mixing oxygen gas with flammable solvents or reagents. More important, introducing two conductors into a flask brings a risk of static electricity discharge between the conductors, which is dangerous whenever a flammable solvent is used without inert gas. As wired metal-gauge digital thermometers are used more often in synthetic practice, precautions must be taken to avoid their contact with other metallic (conducting) parts inside the reaction flasks." (reprint of the full-text)

Explosive

Large (>100g)

Oxidation

安全データ

wgk
-
tsca
TSCA listed
ridadr
UN 1993 3/PG 2
hs_code
29310095
risk_code
11-36/37/38
化審法
(2)-3779

化学と産業

用途と製造

General Manufacturing InformationSilane, ethynyltrimethyl-: ACTIVE
応用分野 · 5 件

用途有機合成原料。

用途有機合成化学では、アリール基に縮合させた後、容易にトリメチルシリル基を除去することができるためアルキニル化アリールを合成するときによく用いられる。アリール基にTMSAをカップリングさせる反応にはヘイカップリングや薗頭カップリングがある。

用途ジチエノチオフェン誘導体の合成。

使用Trimethylsilylacetylene is a valuable reagent used in ethynylation by palladium(0)-catalyzed coupling/condensation with aryl and vinyl halides and triflates, or by nucleophilic attack of the corresponding acetylide on electrophilic centers; reacts with alkyl iodides, tin hydrides,6 and dichloroketene in a regioselective and stereoselective manner, participating in the following synthesis reactions: Ethynylations, Palladium(0)-Catalyzed Coupling Reactions,Reaction of Trimethylsilylacetylides with Electrophiles, Radical-Initiated and Transition Metal-Catalyzed Additions, Cycloaddition Reactions, Ethynylations, Cycloaddition Reactions, Further Transformations etc.

一般的な説明Laser-induced polymerization of gaseous ethynyltrimethylsilane was used for efficient chemical vapour deposition of polycarbosilane films. Ethynyltrimethylsilane acts as substrate for nickel-catalyzed cross-coupling with benzonitriles.

調製方法

純化方法Distil it through an efficient column. The IR has bands at max 2041 (CC) and 3289 (C-H) cm-1. [Kr.hnke & Goss Chem Ber 92 30 1959, Beilstein 4 IV 3937.]

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