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31469-15-5 - 1-Methoxy-2-methyl-1-(trimethylsiloxy)propene, 97% - 1-Methoxy-1-trimethylsiloxy-2-methyl-1-propene - Methyl trimethylsilyl dimethylketene acetal - L06931 - Alfa Aesar

L06931 1-Methoxy-2-methyl-1-(trimethylsiloxy)propene, 97%

Numéro CAS
31469-15-5
Synonymes
1-Methoxy-1-trimethylsiloxy-2-methyl-1-propene
Methyl trimethylsilyl dimethylketene acetal

Dimensions Prix ($) Quantité Disponibilité
5g 64,50
25g 223,00
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1-Methoxy-2-methyl-1-(trimethylsiloxy)propene, 97%

MDL
MFCD00010232
EINECS
000-000-0

Propriétés chimiques

Formule
C8H18O2Si
Poids formulaire
174.32
Point d'ébullition
35-36°/15mm
Point d'éclair
30°(86°F)
Densité
0.858
Indice de réfraction
1.4150
Sensibilité
Moisture Sensitive
Solubilité
Hydrolyzes in water.

Applications

1-Methoxy-2-methyl-1-(trimethylsiloxy)propene is used in the synthesis of chiral β-lactams by reacting with (S)-alkylidene(1-arylethyl)amines in the presence of titanium tetrachloride. It acts as a catalyst or initiator in the group-transfer polymerization. It is also used as a versatile reagent in conjugate addition4 and aldol reactions.

Notes

Moisture Sensitive. Incompatible materials are Strong oxidizing agents and Strong acids. Store in cool place. Keep container tightly closed in a dry and well-ventilated place.

Références bibliographiques

Masahiro Yamanaka; Junji Itoh, Kohei Fuchibe; Takahiko Akiyama. Chiral Brønsted acid catalyzed enantioselective Mannich-type reaction.Journal of the American Chemical Society.2007,129 (21), 6756-6764.

.

Silyl ketene acetal. The silyl enol ether of methyl isobutyrate. Catalyst for the initiation of group transfer polymerization, for controlled polymerization of ɑß-unsaturated esters, ketones, nitriles and amides, in which the ketene acetal function is transferred along the growing polymer chain: J. Am. Chem. Soc., 105, 5706 (1983); Science, 222, 39 (1983).

In the presence of a Lewis acid e.g. TiCl4 or TMS-OTf, undergoes the Mukaiyama aldol reaction with aldehydes to give methyl ɑɑ-dimethyl-ß-hydroxy esters: Chem. Lett., 989 (1975); Synth. Commun., 13, 449 (1983). Excellent results are obtained in these reactions with lanthanide triflates, e.g. Yb(OTf)3, as catalysts: Synthesis, 371 (1993).

With imines, gives ß-amino esters or ß-lactams according to conditions: Tetrahedron Lett., 3643 (1977); Chem. Lett., 1397 (1989); Tetrahedron, 44, 4157 (1988).

Michael additions to enones, catalyzed by Yb(OTf)3, have also been reported: Tetrahedron Lett., 33, 6815 (1992).

Mentions de danger et de prudence du SGH

Mentions de danger (UE): H226-H315-H319-H335

Flammable liquid and vapour. Causes skin irritation. Causes serious eye irritation. May cause respiratory irritation.

Mentions de prudence: P210-P261-P280-P240-P303+P361+P353-P305+P351+P338-P304+P340-P362-P405-P501a

Keep away from heat/sparks/open flames/hot surfaces. - No smoking. Avoid breathing dust/fume/gas/mist/vapours/spray. Wear protective gloves/protective clothing/eye protection/face protection. Ground/bond container and receiving equipment. IF ON SKIN (or hair): Remove/Take off immediately all contaminated clothing. Rinse skin with water/shower. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. IF INHALED: Remove to fresh air and keep at rest in a position comfortable for breathing. Take off contaminated clothing and wash before reuse. Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.

Autres références

Beilstein
1362893
Classe de danger
3
Groupe d'emballage
III
Code tarifaire harmonisé
2931.90
TSCA
No

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