(-)-(2E,4E)-5-[(R)-4-(tert-butyldimethylsilyloxy)-2,6,6-trimethylcyclohex-1-en-1-yl]-3-methylpenta-2,4-dienal

Base Information

Chemical Name:(-)-(2E,4E)-5-[(R)-4-(tert-butyldimethylsilyloxy)-2,6,6-trimethylcyclohex-1-en-1-yl]-3-methylpenta-2,4-dienal
CAS No.:121468-88-0
Molecular Formula:C₂₁H₃₆O₂Si
Molecular Weight:348.601
Hs Code.:

Synonyms:(-)-(2E,4E)-5-[(R)-4-(tert-butyldimethylsilyloxy)-2,6,6-trimethylcyclohex-1-en-1-yl]-3-methylpenta-2,4-dienal

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Chemical Property of (-)-(2E,4E)-5-[(R)-4-(tert-butyldimethylsilyloxy)-2,6,6-trimethylcyclohex-1-en-1-yl]-3-methylpenta-2,4-dienal

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Technology Process of (-)-(2E,4E)-5-[(R)-4-(tert-butyldimethylsilyloxy)-2,6,6-trimethylcyclohex-1-en-1-yl]-3-methylpenta-2,4-dienal

There total 11 articles about (-)-(2E,4E)-5-[(R)-4-(tert-butyldimethylsilyloxy)-2,6,6-trimethylcyclohex-1-en-1-yl]-3-methylpenta-2,4-dienal which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 83.0%

: 875797-47-0
(-)-(2E,4E)-5-[(R)-4-(tert-butyldimethylsilyloxy)-2,6,6-trimethylcyclohex-1-en-1-yl]-3-methylpenta-2,4-dien-1-ol

: 121468-88-0
(-)-(2E,4E)-5-[(R)-4-(tert-butyldimethylsilyloxy)-2,6,6-trimethylcyclohex-1-en-1-yl]-3-methylpenta-2,4-dienal

Guidance literature:: With tetrapropylammonium perruthennate; 4 A molecular sieve; 4-methylmorpholine N-oxide; In dichloromethane; at 25 ℃; for 3h;
DOI:10.1039/b514273c

Reference yield:

: 128426-10-8
(2E,4E)-5-(tri-n-butylstannyl)-3-methylpenta-2,4-dien-1-ol

: 121468-88-0
(-)-(2E,4E)-5-[(R)-4-(tert-butyldimethylsilyloxy)-2,6,6-trimethylcyclohex-1-en-1-yl]-3-methylpenta-2,4-dienal

Guidance literature:: Multi-step reaction with 2 steps

1: 68 percent / AsPh₃; LiCl / Pd₂(dba)3 / 1-methyl-pyrrolidin-2-one / 14 h / 80 °C

2: 83 percent / N-methylmorpholine N-oxide; 4 Angstroem molecular sieves; tetra-n-propylammonium perruthenate / CH₂Cl₂ / 3 h / 25 °C

With tetrapropylammonium perruthennate; triphenyl-arsane; 4 A molecular sieve; 4-methylmorpholine N-oxide; lithium chloride; tris(dibenzylideneacetone)dipalladium ⁽⁰⁾; In 1-methyl-pyrrolidin-2-one; dichloromethane; 1: Stille cross coupling;
DOI:10.1039/b514273c

Reference yield:

: 152187-06-9
(R)-5-(tert-butyldimethylsilyloxy)-2-[(trifluoromethanesulfonyl)oxy]-1,3,3-trimethylcyclohex-1-ene

: 121468-88-0
(-)-(2E,4E)-5-[(R)-4-(tert-butyldimethylsilyloxy)-2,6,6-trimethylcyclohex-1-en-1-yl]-3-methylpenta-2,4-dienal

Guidance literature:: Multi-step reaction with 2 steps

1: 68 percent / AsPh₃; LiCl / Pd₂(dba)3 / 1-methyl-pyrrolidin-2-one / 14 h / 80 °C

2: 83 percent / N-methylmorpholine N-oxide; 4 Angstroem molecular sieves; tetra-n-propylammonium perruthenate / CH₂Cl₂ / 3 h / 25 °C

With tetrapropylammonium perruthennate; triphenyl-arsane; 4 A molecular sieve; 4-methylmorpholine N-oxide; lithium chloride; tris(dibenzylideneacetone)dipalladium ⁽⁰⁾; In 1-methyl-pyrrolidin-2-one; dichloromethane; 1: Stille cross coupling;
DOI:10.1039/b514273c