(2E)-7-{[(4-methylphenyl)sulfonyl]amino}-1,7-diphenylhept-2-en-1-yl acetate

Base Information

Chemical Name:(2E)-7-{[(4-methylphenyl)sulfonyl]amino}-1,7-diphenylhept-2-en-1-yl acetate
CAS No.:1221972-25-3
Molecular Formula:C₂₈H₃₁NO₄S
Molecular Weight:477.624
Hs Code.:

Synonyms:(2E)-7-{[(4-methylphenyl)sulfonyl]amino}-1,7-diphenylhept-2-en-1-yl acetate

Suppliers and Price of (2E)-7-{[(4-methylphenyl)sulfonyl]amino}-1,7-diphenylhept-2-en-1-yl acetate

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (2E)-7-{[(4-methylphenyl)sulfonyl]amino}-1,7-diphenylhept-2-en-1-yl acetate

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Technology Process of (2E)-7-{[(4-methylphenyl)sulfonyl]amino}-1,7-diphenylhept-2-en-1-yl acetate

There total 1 articles about (2E)-7-{[(4-methylphenyl)sulfonyl]amino}-1,7-diphenylhept-2-en-1-yl acetate 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: 65.0%

: 7217-71-2
1-phenyl-2-propenyl acetate

: 1221972-17-3
4-methyl-N-(1-phenylhex-5-en-1-yl)benzenesulfonamide

: 1221972-25-3
(2E)-7-{[(4-methylphenyl)sulfonyl]amino}-1,7-diphenylhept-2-en-1-yl acetate

Guidance literature:: With Hoveyda-Grubbs catalyst second generation; In dichloromethane; at 40 ℃;
DOI:10.1021/ol100422d

Reference yield:

: 1221972-25-3
(2E)-7-{[(4-methylphenyl)sulfonyl]amino}-1,7-diphenylhept-2-en-1-yl acetate

: trans-2-phenyl-6-((E)-styryl)-1-(toluene-4-sulfonyl)-piperidine

: cis-2-phenyl-6-((E)-styryl)-1-(toluene-4-sulfonyl)-piperidine

Guidance literature:: With iron(III) chloride hexahydrate; In dichloromethane; at 20 ℃; for 0.5h; optical yield given as %de; diastereoselective reaction;
DOI:10.1021/ol100422d