1-methyl-7,10,11-triphenyl-cis-transoid-1,2-cie-2-transoid-2,3-cis-3-4,8,9-trioxatetracyclo<4,2,2,0,0>undec-10-ene

Base Information

Chemical Name:1-methyl-7,10,11-triphenyl-cis-transoid-1,2-cie-2-transoid-2,3-cis-3-4,8,9-trioxatetracyclo<4,2,2,0,0>undec-10-ene
CAS No.:79491-06-8
Molecular Formula:C₂₇H₂₂O₃
Molecular Weight:394.47
Hs Code.:

Synonyms:1-methyl-7,10,11-triphenyl-cis-transoid-1,2-cie-2-transoid-2,3-cis-3-4,8,9-trioxatetracyclo<4,2,2,0,0>undec-10-ene

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Chemical Property of 1-methyl-7,10,11-triphenyl-cis-transoid-1,2-cie-2-transoid-2,3-cis-3-4,8,9-trioxatetracyclo<4,2,2,0,0>undec-10-ene

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Technology Process of 1-methyl-7,10,11-triphenyl-cis-transoid-1,2-cie-2-transoid-2,3-cis-3-4,8,9-trioxatetracyclo<4,2,2,0,0>undec-10-ene

There total 3 articles about 1-methyl-7,10,11-triphenyl-cis-transoid-1,2-cie-2-transoid-2,3-cis-3-4,8,9-trioxatetracyclo<4,2,2,0,0>undec-10-ene 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: 96.0%

: 67723-29-9,79548-32-6
2-methyl-3,4,5-triphenyl-cis-transoid-1,9-cis-7,8-oxatricyclo<4,3,0,0>nona-2,4-diene

: 79491-06-8
1-methyl-7,10,11-triphenyl-cis-transoid-1,2-cie-2-transoid-2,3-cis-3-4,8,9-trioxatetracyclo<4,2,2,0,0>undec-10-ene

Guidance literature:: With Eosin Y; oxygen; In ethanol; chloroform; for 20h; Irradiation;

Reference yield:

: 67723-27-7
dibenzyl 1-methyl-6,9,10-triphenyl-cis-transoid-1,2-cis-2-7-8-diazatricyclo<4,2,2,0>deca-3,9-diene-7,8-dicarboxylate

: 79491-06-8
1-methyl-7,10,11-triphenyl-cis-transoid-1,2-cie-2-transoid-2,3-cis-3-4,8,9-trioxatetracyclo<4,2,2,0,0>undec-10-ene

Guidance literature:: Multi-step reaction with 3 steps

1: 77 percent / 3-chloroperbenzoic acid / CHCl₃ / 4.5 h / Heating

2: 2.) red mercuric oxide / 1.) 10 percent palladium on charcoal / 1.) ethyl acetate, RT, 2.) ethyl acetate, 22 h

3: 96 percent / eosin, O₂ / CHCl₃; ethanol / 20 h / Irradiation

With Eosin Y; oxygen; 3-chloro-benzenecarboperoxoic acid; mercury(II) oxide; palladium on activated charcoal; In ethanol; chloroform;

Reference yield:

: 67723-28-8
dibenzyl 1-methyl-7,10,11-triphenyl-cis-transoid-1,2-cis-2-transoid-2,3-cis-3-8,9-diaza-4-oxatetracyclo<5,2,2,0,0>undec-10-ene-8,9-dicarboxylate

: 79491-06-8
1-methyl-7,10,11-triphenyl-cis-transoid-1,2-cie-2-transoid-2,3-cis-3-4,8,9-trioxatetracyclo<4,2,2,0,0>undec-10-ene

Guidance literature:: Multi-step reaction with 2 steps

1: 2.) red mercuric oxide / 1.) 10 percent palladium on charcoal / 1.) ethyl acetate, RT, 2.) ethyl acetate, 22 h

2: 96 percent / eosin, O₂ / CHCl₃; ethanol / 20 h / Irradiation

With Eosin Y; oxygen; mercury(II) oxide; palladium on activated charcoal; In ethanol; chloroform;