((Z)-4-{(1S,2R,3S,4R)-3-[(E)-(3R,4S)-4-Phenyl-3-(tetrahydro-pyran-2-yloxy)-pent-1-enyl]-7-oxa-bicyclo[2.2.1]hept-2-yl}-but-2-enyloxy)-acetic acid tert-butyl ester

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Chemical Name:((Z)-4-{(1S,2R,3S,4R)-3-[(E)-(3R,4S)-4-Phenyl-3-(tetrahydro-pyran-2-yloxy)-pent-1-enyl]-7-oxa-bicyclo[2.2.1]hept-2-yl}-but-2-enyloxy)-acetic acid tert-butyl ester
CAS No.:104101-53-3
Molecular Formula:C₃₂H₄₆O₆
Molecular Weight:526.714
Hs Code.:

Synonyms:((Z)-4-{(1S,2R,3S,4R)-3-[(E)-(3R,4S)-4-Phenyl-3-(tetrahydro-pyran-2-yloxy)-pent-1-enyl]-7-oxa-bicyclo[2.2.1]hept-2-yl}-but-2-enyloxy)-acetic acid tert-butyl ester

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Chemical Property of ((Z)-4-{(1S,2R,3S,4R)-3-[(E)-(3R,4S)-4-Phenyl-3-(tetrahydro-pyran-2-yloxy)-pent-1-enyl]-7-oxa-bicyclo[2.2.1]hept-2-yl}-but-2-enyloxy)-acetic acid tert-butyl ester

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Technology Process of ((Z)-4-{(1S,2R,3S,4R)-3-[(E)-(3R,4S)-4-Phenyl-3-(tetrahydro-pyran-2-yloxy)-pent-1-enyl]-7-oxa-bicyclo[2.2.1]hept-2-yl}-but-2-enyloxy)-acetic acid tert-butyl ester

There total 5 articles about ((Z)-4-{(1S,2R,3S,4R)-3-[(E)-(3R,4S)-4-Phenyl-3-(tetrahydro-pyran-2-yloxy)-pent-1-enyl]-7-oxa-bicyclo[2.2.1]hept-2-yl}-but-2-enyloxy)-acetic acid tert-butyl ester 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: 67.0%

: 5292-43-3
bromoacetic acid tert-butyl ester

: 104153-89-1
(Z)-5-{(1S,2R,3S,4R)-3-[(E)-(3R,4S)-4-Phenyl-3-(tetrahydro-pyran-2-yloxy)-pent-1-enyl]-7-oxa-bicyclo[2.2.1]hept-2-yl}-pent-3-en-1-ol

: 104101-53-3
((Z)-4-{(1S,2R,3S,4R)-3-[(E)-(3R,4S)-4-Phenyl-3-(tetrahydro-pyran-2-yloxy)-pent-1-enyl]-7-oxa-bicyclo[2.2.1]hept-2-yl}-but-2-enyloxy)-acetic acid tert-butyl ester

Guidance literature:: With sodium hydroxide; n-BuNHSO₄; In tetrahydrofuran; at 25 ℃; for 5h;
DOI:10.1021/jm00168a032

Reference yield:

: 126451-84-1
1S-<1α,2α,3α(E,3S^*,4R^*),4α>-7-<3-<4-phenyl-3-(tetrahydropyranyloxy)-1-pentenyl>-7-oxabicyclo<2.2.1>hept-2-yl>acetaldehyde

: 104101-53-3
((Z)-4-{(1S,2R,3S,4R)-3-[(E)-(3R,4S)-4-Phenyl-3-(tetrahydro-pyran-2-yloxy)-pent-1-enyl]-7-oxa-bicyclo[2.2.1]hept-2-yl}-but-2-enyloxy)-acetic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 43 percent / methanol / 5 h / 25 °C

2: 94 percent / diisobutylaluminum hydride / tetrahydrofuran; toluene / 2 h / -78 °C

3: 67 percent / n-BuNHSO₄, 50percent aq. NaOH / tetrahydrofuran / 5 h / 25 °C

With sodium hydroxide; n-BuNHSO₄; diisobutylaluminium hydride; In tetrahydrofuran; methanol; toluene;
DOI:10.1021/jm00168a032

Reference yield:

: 104101-47-5
5,6-Dihydroxy-7-{(1S,2R,3S,4R)-3-[(E)-(3R,4S)-4-phenyl-3-(tetrahydro-pyran-2-yloxy)-pent-1-enyl]-7-oxa-bicyclo[2.2.1]hept-2-yl}-heptanoic acid methyl ester

: 104101-53-3
((Z)-4-{(1S,2R,3S,4R)-3-[(E)-(3R,4S)-4-Phenyl-3-(tetrahydro-pyran-2-yloxy)-pent-1-enyl]-7-oxa-bicyclo[2.2.1]hept-2-yl}-but-2-enyloxy)-acetic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: sodium metaperiodate / methanol; H₂O / 2 h / 25 °C

2: 43 percent / methanol / 5 h / 25 °C

3: 94 percent / diisobutylaluminum hydride / tetrahydrofuran; toluene / 2 h / -78 °C

4: 67 percent / n-BuNHSO₄, 50percent aq. NaOH / tetrahydrofuran / 5 h / 25 °C

With sodium hydroxide; sodium periodate; n-BuNHSO₄; diisobutylaluminium hydride; In tetrahydrofuran; methanol; water; toluene;
DOI:10.1021/jm00168a032