(1S,3S) and (1R,3S)-2-(4-benzyloxy-3-methoxy-phenyl)-1-[2-(3,7-dimethyl-oct-6-enyl)-[1,3]dithian-2-yl]-ethanol

Base Information

Chemical Name:(1S,3S) and (1R,3S)-2-(4-benzyloxy-3-methoxy-phenyl)-1-[2-(3,7-dimethyl-oct-6-enyl)-[1,3]dithian-2-yl]-ethanol
CAS No.:915695-44-2
Molecular Formula:C₃₀H₄₂O₃S₂
Molecular Weight:514.794
Hs Code.:

Synonyms:(1S,3S) and (1R,3S)-2-(4-benzyloxy-3-methoxy-phenyl)-1-[2-(3,7-dimethyl-oct-6-enyl)-[1,3]dithian-2-yl]-ethanol

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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 (1S,3S) and (1R,3S)-2-(4-benzyloxy-3-methoxy-phenyl)-1-[2-(3,7-dimethyl-oct-6-enyl)-[1,3]dithian-2-yl]-ethanol

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Technology Process of (1S,3S) and (1R,3S)-2-(4-benzyloxy-3-methoxy-phenyl)-1-[2-(3,7-dimethyl-oct-6-enyl)-[1,3]dithian-2-yl]-ethanol

There total 1 articles about (1S,3S) and (1R,3S)-2-(4-benzyloxy-3-methoxy-phenyl)-1-[2-(3,7-dimethyl-oct-6-enyl)-[1,3]dithian-2-yl]-ethanol 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: 96.6%

: 915695-61-3
(3S)-2-(4-benzyloxy-3-methoxy-phenyl)-1-[2-(3,7-dimethyl-oct-6-enyl)-[1,3]dithian-2-yl]-ethanone

: 915695-44-2
(1S,3S) and (1R,3S)-2-(4-benzyloxy-3-methoxy-phenyl)-1-[2-(3,7-dimethyl-oct-6-enyl)-[1,3]dithian-2-yl]-ethanol

Guidance literature:: With sodium tetrahydroborate; In methanol; at 20 ℃; for 0.5h;

Reference yield: 79.0%

: 915695-44-2
(1S,3S) and (1R,3S)-2-(4-benzyloxy-3-methoxy-phenyl)-1-[2-(3,7-dimethyl-oct-6-enyl)-[1,3]dithian-2-yl]-ethanol

: 915695-43-1
(2R,6S) and (2S,6S)-1-(4-benzyloxy-3-methoxy-phenyl)-2-hydroxy-6,10-dimethyl-undec-9-en-3-one

Guidance literature:: With water; sodium hydrogencarbonate; methyl iodide; In acetone; acetonitrile; at 60 ℃; for 18h; Product distribution / selectivity;