Skip to Content
Merck
All Photos(1)

Key Documents

212830

Sigma-Aldrich

trans-1-Methoxy-3-trimethylsiloxy-1,3-butadiene

95%

Synonym(s):

Danishefsky’s diene

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
(CH3)3SiOC(=CH2)CH=CHOCH3
CAS Number:
Molecular Weight:
172.30
Beilstein:
1616761
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

95%

form

liquid

impurities

2-5% 4-methoxy-3-buten-2-one

refractive index

n20/D 1.454 (lit.)

bp

68-69 °C/14 mmHg (lit.)

density

0.885 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

CO\C=C\C(=C)O[Si](C)(C)C

InChI

1S/C8H16O2Si/c1-8(6-7-9-2)10-11(3,4)5/h6-7H,1H2,2-5H3/b7-6+

InChI key

SHALBPKEGDBVKK-VOTSOKGWSA-N

Looking for similar products? Visit Product Comparison Guide

General description

trans-1-methoxy-3-trimethylsiloxy-1,3-butadiene is a funtionalized Diels-Alder diene. Mukaiyama-Michael-type addition/heterocyclization of trans-1-methoxy-3-trimethylsiloxy-1,3-butadiene (Danishefsky′s diene) with 1,2-diaza-1,3-butadiene has been investigated. Asymmetric hetero-Diels-Alder cyclization of Danishefsky′s diene with benzaldehyde catalyzed by mesoporous inorganic/metalorganic hybrid materials has been reported.

Application

trans-1-Methoxy-3-trimethylsiloxy-1,3-butadiene was used:
  • in the synthesis of sulfone analogues of griseofulvin (sulfogriseofulvins), 4H-1-aminopyrroles and 4,5H-pyrazoles
  • as Diels-Alder diene for the synthesis of pyridones and pyranones
  • as reagent employed in the Mannich-Michael reaction for preparation of piperidinones and enaminones

Pictograms

Flame

Signal Word

Warning

Hazard Statements

Hazard Classifications

Flam. Liq. 3

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

138.2 °F - closed cup

Flash Point(C)

59 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Mingji Dai et al.
Journal of the American Chemical Society, 129(3), 645-657 (2007-01-18)
The paper describes the course of cycloadditions of Diels-Alder dienophiles containing linked enyne sites, each substituted with activating groups. Consistently, it was found that in the enyne cases the Diels-Alder reaction occurred specifically at the acetylenic center. Furthermore, it was
Tetrahedron, 49, 1749-1749 (1993)
The Journal of Organic Chemistry, 57, 3605-3605 (1992)
The Journal of Organic Chemistry, 57, 4444-4444 (1992)
M Friedrich et al.
Archiv der Pharmazie, 329(7), 361-370 (1996-07-01)
Syntheses of substituted, especially of fluoro substituted benzoxathiole 1,1-dioxides, are described. These derivatives were transformed via the Peterson olefination into substituted 2-alkylidene derivatives 27. Diels-Alder reactions of 27 with 1,1-dimethoxy- and 1-methoxy-3-trimethylsiloxy-1,3-butadiene (30, 32) gave sulfone analogues 31 of griseofulvin

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service