トリメチルシリルアジド

Azidotrimethylsilane

HCID 78378CAS 4648-54-8

基本情報

標準SMILES
C[Si](C)(C)N=[N+]=[N-]
InChIKey
SEDZOYHHAIAQIW-UHFFFAOYSA-N
分子式
C3H9N3Si
平均分子量
115.21 g/mol

概要

structure in first source

名称と識別子

優先名称
Azidotrimethylsilane
IUPAC
azido(trimethyl)silane
現地名
トリメチルシリルアジド
英語名
Azidotrimethylsilane
分子式
C3H9N3Si
分子量
115.21

名称と別名

azidotrimethylsilaneTrimethylsilyl azide4648-54-8Silane, azidotrimethyl-EM57JSM2Y9Me3SiN3DTXSID3063542RefChem:116112DTXCID7040493225-078-5Trimethylsilylazideazido(trimethyl)silane
名称をさらに表示
トリメチルシリルアジド1-(トリメチルシリル)-1,3-ジアザ-2-アゾニアプロパジエン-3-イド(トリメチルシリル)アザイドアジドトリメチルシラントリメチルシリルアザイドトリメチルアジドシランアジド(トリメチル)シランTMSN3TMSiAdecomposes(CH3)3SiN3AzidotrimethyLThree methyl azide silaneCFS-548Co-Formula CFS-548
MFCD00001986Trimethylazidosilane; Trimethylsilicon azide; Trimethylsilyl azideC3H9N3SitrimethylazidosilaneCCRIS 8048TMS azideTMS-azidetrimethyl silylazide

データベース識別子

CAS
4648-54-8
PubChem CID
78378
DTXSID
DTXSID3063542
UNII
EM57JSM2Y9
EC Number
225-078-5
Nikkaji
J80.870I

物性

構造計算による物性

極性表面積
14.4 Ų
水素結合供与体数
0
水素結合受容体数
2
回転可能結合数
1
重原子数
7

実験および物理化学的性質

Chemical ClassesMetals -> Metalloid Compounds (Silicon)
Physical DescriptionColorless liquid; [Alfa Aesar MSDS]

物理化学的性質

融点
-95 °C · -95°C
沸点
92 · 92-95 °C(lit.)
比重(密度)
0.876 g/mL · 0.876 g/mL at 20 °C(lit.)
屈折率
20 · n20/D 1.415(lit.)
闪点
74 °F · 74 °F
貯蔵温度
2 · 2-8°C
化学的性質 · 1 件

化学的特性Azidotrimethylsilane (TMSN3) is a clear colorless to slightly yellow liquid. It shows very slow decomposition at high temperatures. It is a very commonly used azide source and has been used in the synthesis of aminotriazole ligands. Azidotrimethylsilane can be easily synthesised by adding chlorotrimethylsilane dropwise to a stirred solution of NaN3 in diethylene glycol dimethyl ether.

安全と法規制

GHS分類

GHS Classification · 4 件

Danger

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

P210, P233, P240, P241, P242, P243, P261, P262, P264, P270, P271, P273, P280, P301+P316, P302+P352, P303+P361+P353, P304+P340, P316, P321, P330, P361+P364, P370+P378, P391, P403+P233, P403+P235, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 52 reports by companies from 7 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

危険有害性情報

Regulatory Information · 3 件

Chemical: Silane, azidotrimethyl-

Status: Active Update: 09-04-2018 https://echa.europa.eu/registration-dossier/-/registered-dossier/23688

Trimethylsilyl azide: Does not have an individual approval but may be used under an appropriate group standard

Hazards SummaryReacts with water evolving toxic gases; May cause irritation; Toxic by ingestion, inhalation, and skin absorption; [Alfa Aesar MSDS] See Hexamethyldisilazane. See Sodium azide.
Hazard Classes and CategoriesFlam. Liq. 2 (100%)
CSL Reaction Information · 6 件

CSL00010

BORON TRIFLUORIDE + AZIDOTRIMETHYLSILANE

Combinations of TMSN3 and Lewis acids can detonate, presumably due to formation of HN3 from residual water. Avoid Lewis acids.

Explosive

Cycloaddition

User-Reported

安全データ

F
10-33
wgk
3
tsca
TSCA listed
ridadr
UN 1992 3/PG 2
hs_code
29310095
risk_code
11-23/24/25-50/53-29

化学と産業

用途と製造

General Manufacturing InformationSilane, azidotrimethyl-: ACTIVE
応用分野 · 2 件

用途有機合成原料。

使用Many applications of TMSA in organic synthesis have been reported but only representative examples are described herein.Substitution Reactions. Benzyl,allyl,and substituted alkyl halides are converted to the corresponding azides in 60–100% yields via reactions with TMSA under neutral conditions in a nonaqueous solvent (eq 1).By using tin(IV) chloride as a catalyst, secondary and tertiary cyclic and polycyclic halides are similarly transformed into the corresponding azides in 50–92% yields (eq 1).

調製方法 · 2 件

製造方法Azidotrimethylsilane may be synthesised by reacting trimethylchlorosilane with sodium azide in hexamethylphosphoramidic triamide. several methods for the synthesis of this azide have been reported.The procedure involving aluminum chloride is not recommended, since an explosive product is formed.Azidotrimethylsilane is now commercially available, and a representative synthetic procedure is as follows. A mixture of sodium azide and chlorotrimethylsilane is refluxed in di-n-butyl ether for 2 days and the azide is safely distilled directly from the reaction vessel. Purer compound (99% content) is obtained by redistillation of the product. Several improved conditions have been reported for the preparation of this azide.In these procedures, trimethylsilyl chloride is reacted with sodium azide either neat or in a high boiling point solvent, such as a mixture of silicone oil and polyethylene glycol. Distillation of the crude product usually provides trimethylsilyl azide (TMSA) in high purity (97.9%) and yield (97%).

純化方法Distil the azide through a Vigreux column (p 11) in a N2 atmosphere maintaining the oil bath temperature thermostat at 135-140o . Check the purity by 1H NMR [CHCl3, : single peak at 13cps from Me4Si]. Likely impurities are siloxane hydrolysis products. The azide is thermally stable even at 200o when it decomposes slowly without explosive violence. All the same, it is advisable to carry out the distillation behind a thick safety screen in a fumehood because unforseen EXPLOSIVE azides may be formed on long standing. [Birkofer & Wagner Org Synth Coll Vol VI 1030 1988.]

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