(4R,6R)-2-<(tert-butyldimethylsilyl)oxy>-4-methyl-6-(phenylsulfonyl)-2(E)-heptene

Base Information

Chemical Name:(4R,6R)-2-<(tert-butyldimethylsilyl)oxy>-4-methyl-6-(phenylsulfonyl)-2(E)-heptene
CAS No.:104996-27-2
Molecular Formula:C₂₀H₃₄O₃SSi
Molecular Weight:382.64
Hs Code.:

Synonyms:(4R,6R)-2-<(tert-butyldimethylsilyl)oxy>-4-methyl-6-(phenylsulfonyl)-2(E)-heptene

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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 (4R,6R)-2-<(tert-butyldimethylsilyl)oxy>-4-methyl-6-(phenylsulfonyl)-2(E)-heptene

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Technology Process of (4R,6R)-2-<(tert-butyldimethylsilyl)oxy>-4-methyl-6-(phenylsulfonyl)-2(E)-heptene

There total 5 articles about (4R,6R)-2-<(tert-butyldimethylsilyl)oxy>-4-methyl-6-(phenylsulfonyl)-2(E)-heptene 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: 95.0%

: 18162-48-6
tert-butyldimethylsilyl chloride

: 104705-92-2
(4R,6R)-4-methyl-6-(phenylsulfonyl)-2(E)-hepten-1-ol

: 104996-27-2
(4R,6R)-2-<(tert-butyldimethylsilyl)oxy>-4-methyl-6-(phenylsulfonyl)-2(E)-heptene

Guidance literature:: With 1H-imidazole; In N,N-dimethyl-formamide; for 2h; Ambient temperature;
DOI:10.1021/jo00375a017

Reference yield:

: 14204-27-4
N-phenylthiophthalimide

: 104996-27-2
(4R,6R)-2-<(tert-butyldimethylsilyl)oxy>-4-methyl-6-(phenylsulfonyl)-2(E)-heptene

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) (n-Bu)3P / 1.) benzene, 10 min, 2.) benzene, 3 h

2: 87 percent / (i-Bu)2AlH / toluene / 0.17 h / -6 °C

3: 88 percent / oxone / H₂O; methanol / 2 h / Ambient temperature

4: 95 percent / imidazole / dimethylformamide / 2 h / Ambient temperature

With 1H-imidazole; Oxone; tributylphosphine; diisobutylaluminium hydride; In methanol; water; N,N-dimethyl-formamide; toluene;
DOI:10.1021/jo00375a017

Reference yield:

: 104996-26-1
(4R,6R)-4-methyl-6-(phenylthio)-2(E)-hepten-1-ol

: 104996-27-2
(4R,6R)-2-<(tert-butyldimethylsilyl)oxy>-4-methyl-6-(phenylsulfonyl)-2(E)-heptene

Guidance literature:: Multi-step reaction with 2 steps

1: 88 percent / oxone / H₂O; methanol / 2 h / Ambient temperature

2: 95 percent / imidazole / dimethylformamide / 2 h / Ambient temperature

With 1H-imidazole; Oxone; In methanol; water; N,N-dimethyl-formamide;
DOI:10.1021/jo00375a017