Technology Process of (2R,4S,5R,6R,7R,8R,12S,13S)-1-(benzyloxy)-2,4,12-trihydroxy-5,7-dimethyl-10-methylidene-8-{(1R)-1-[4-(trifluoromethyl)phenyl]ethoxy}-13-[(4S,5S,6R)-2,2,5-trimethyl-6-(propan-2-yl)-1,3-dioxan-4-yl]tetradecan-6-yl 4-methoxybenzoate
There total 7 articles about (2R,4S,5R,6R,7R,8R,12S,13S)-1-(benzyloxy)-2,4,12-trihydroxy-5,7-dimethyl-10-methylidene-8-{(1R)-1-[4-(trifluoromethyl)phenyl]ethoxy}-13-[(4S,5S,6R)-2,2,5-trimethyl-6-(propan-2-yl)-1,3-dioxan-4-yl]tetradecan-6-yl 4-methoxybenzoate 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:
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1298085-84-3
(2S,3S,7R,8S,9R,10R,11S,13R)-14-(benzyloxy)-13-[(4-methoxybenzyl)oxy]-8,10-dimethyl-5-methylidene-7-{(1R)-1-[4-(trifluoromethyl)phenyl]ethoxy}-2-[(4S,5S,6R)-2,2,5-trimethyl-6-(propan-2-yl)-1,3-dioxan-4-yl]tetradecane-3,9,11-triol
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1298085-87-6
(2R,4S,5R,6R,7S,8R,12S,13S)-1-(benzyloxy)-5,77-dimethyl-10-methylidene-8-{(1R)-1-[4-(trifluoromethyl)phenyl]ethoxy}-13-[(4S,5S,6R)-2,2,5-trimethyl-6-(propan-2-yl)-1,3-dioxan-4-yl]tetradecane-2,4,6,12-tetrol
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1298086-01-7
(2R,4S,5R,6R,7R,8R,12S,13S)-1-(benzyloxy)-2,4,12-trihydroxy-5,7-dimethyl-10-methylidene-8-{(1R)-1-[4-(trifluoromethyl)phenyl]ethoxy}-13-[(4S,5S,6R)-2,2,5-trimethyl-6-(propan-2-yl)-1,3-dioxan-4-yl]tetradecan-6-yl 4-methoxybenzoate
- Guidance literature:
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With
2,3-dicyano-5,6-dichloro-p-benzoquinone;
In
dichloromethane;
at 0 - 20 ℃;
for 5h;
Inert atmosphere;
Molecular sieve;
DOI:10.1002/chem.201003264
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1298086-01-7
(2R,4S,5R,6R,7R,8R,12S,13S)-1-(benzyloxy)-2,4,12-trihydroxy-5,7-dimethyl-10-methylidene-8-{(1R)-1-[4-(trifluoromethyl)phenyl]ethoxy}-13-[(4S,5S,6R)-2,2,5-trimethyl-6-(propan-2-yl)-1,3-dioxan-4-yl]tetradecan-6-yl 4-methoxybenzoate
- Guidance literature:
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Multi-step reaction with 9 steps
1.1: trimethylsilyl trifluoromethanesulfonate / toluene / 6 h / -78 °C / Inert atmosphere
1.2: 16 h / -78 °C / Inert atmosphere
1.3: 0.33 h / Inert atmosphere; Reflux
2.1: pentamethylbenzene,; boron trichloride / dichloromethane / -78 °C / Inert atmosphere
3.1: lithium hexamethyldisilazane / tetrahydrofuran / 0.58 h / -78 °C / Inert atmosphere
3.2: 0.5 h / -78 °C / Inert atmosphere
4.1: boron trifluoride diethyl etherate / dichloromethane / 2.5 h / -78 °C / Inert atmosphere
5.1: diethyl methoxy borane / tetrahydrofuran; methanol / 0.33 h / -78 °C / Inert atmosphere
5.2: Inert atmosphere
6.1: toluene-4-sulfonic acid / 0.5 h / 20 °C / Inert atmosphere
7.1: methyllithium lithium bromide / 1,2-dimethoxyethane; diethyl ether / 0.75 h / -78 °C / Inert atmosphere
7.2: 1.5 h / -78 °C / Inert atmosphere
8.1: tetramethylammonium triacetoxyborohydride / acetic acid; acetonitrile / -40 - 20 °C / Inert atmosphere
9.1: 2,3-dicyano-5,6-dichloro-p-benzoquinone / dichloromethane / 5 h / 0 - 20 °C / Inert atmosphere; Molecular sieve
With
methyllithium lithium bromide; trimethylsilyl trifluoromethanesulfonate; pentamethylbenzene,; diethyl methoxy borane; boron trifluoride diethyl etherate; boron trichloride; toluene-4-sulfonic acid; 2,3-dicyano-5,6-dichloro-p-benzoquinone; lithium hexamethyldisilazane; tetramethylammonium triacetoxyborohydride;
In
tetrahydrofuran; methanol; 1,2-dimethoxyethane; diethyl ether; dichloromethane; acetic acid; toluene; acetonitrile;
4.1: Mukaiyama reaction;
DOI:10.1002/chem.201003264
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1298085-78-5
(2Z,4R,5R,9S,10S,12S,13R)-13-hydroxy-4,10,12,14-tetramethyl-7-methylidene-11-oxo-5-{(1R)-1-[4-(trifluoromethyl)phenyl]ethoxy}pentadec-2-ene-3,9-diyl dibenzoate
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1298086-01-7
(2R,4S,5R,6R,7R,8R,12S,13S)-1-(benzyloxy)-2,4,12-trihydroxy-5,7-dimethyl-10-methylidene-8-{(1R)-1-[4-(trifluoromethyl)phenyl]ethoxy}-13-[(4S,5S,6R)-2,2,5-trimethyl-6-(propan-2-yl)-1,3-dioxan-4-yl]tetradecan-6-yl 4-methoxybenzoate
- Guidance literature:
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Multi-step reaction with 5 steps
1.1: diethyl methoxy borane / tetrahydrofuran; methanol / 0.33 h / -78 °C / Inert atmosphere
1.2: Inert atmosphere
2.1: toluene-4-sulfonic acid / 0.5 h / 20 °C / Inert atmosphere
3.1: methyllithium lithium bromide / 1,2-dimethoxyethane; diethyl ether / 0.75 h / -78 °C / Inert atmosphere
3.2: 1.5 h / -78 °C / Inert atmosphere
4.1: tetramethylammonium triacetoxyborohydride / acetic acid; acetonitrile / -40 - 20 °C / Inert atmosphere
5.1: 2,3-dicyano-5,6-dichloro-p-benzoquinone / dichloromethane / 5 h / 0 - 20 °C / Inert atmosphere; Molecular sieve
With
methyllithium lithium bromide; diethyl methoxy borane; toluene-4-sulfonic acid; 2,3-dicyano-5,6-dichloro-p-benzoquinone; tetramethylammonium triacetoxyborohydride;
In
tetrahydrofuran; methanol; 1,2-dimethoxyethane; diethyl ether; dichloromethane; acetic acid; acetonitrile;
DOI:10.1002/chem.201003264