(3R,5R)-5-[1,3]Dithian-2-yl-3-(4-methoxy-benzyloxy)-2,2-dimethyl-hexan-1-ol

Base Information

Chemical Name:(3R,5R)-5-[1,3]Dithian-2-yl-3-(4-methoxy-benzyloxy)-2,2-dimethyl-hexan-1-ol
CAS No.:215317-78-5
Molecular Formula:C₂₀H₃₂O₃S₂
Molecular Weight:384.604
Hs Code.:

Synonyms:(3R,5R)-5-[1,3]Dithian-2-yl-3-(4-methoxy-benzyloxy)-2,2-dimethyl-hexan-1-ol

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Chemical Property of (3R,5R)-5-[1,3]Dithian-2-yl-3-(4-methoxy-benzyloxy)-2,2-dimethyl-hexan-1-ol

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Technology Process of (3R,5R)-5-[1,3]Dithian-2-yl-3-(4-methoxy-benzyloxy)-2,2-dimethyl-hexan-1-ol

There total 10 articles about (3R,5R)-5-[1,3]Dithian-2-yl-3-(4-methoxy-benzyloxy)-2,2-dimethyl-hexan-1-ol 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: 73.0%

: 215317-77-4
(4R)-4-((2R)-5-m-dithian-2-ylpropyl)-2-(p-methoxyphenyl)-5,5-dimethyl-m-dioxane

: 215317-78-5
(3R,5R)-5-[1,3]Dithian-2-yl-3-(4-methoxy-benzyloxy)-2,2-dimethyl-hexan-1-ol

Guidance literature:: With diisobutylaluminium hydride; In hexane; dichloromethane; at 0 - 20 ℃;
DOI:10.1021/jo981083t

Reference yield:

: 104708-02-3
2-Methyl-2-(S)-oxiranyl-propan-1-ol

: 215317-78-5
(3R,5R)-5-[1,3]Dithian-2-yl-3-(4-methoxy-benzyloxy)-2,2-dimethyl-hexan-1-ol

Guidance literature:: Multi-step reaction with 9 steps

1: 95 percent / imidazole / CH₂Cl₂ / 2.5 h

2: 72 percent / 1,2-dimethoxy-ethane; hexane / Heating

3: 81 percent / LiHMDS / tetrahydrofuran / -78 °C

4: 96 percent / LDA / tetrahydrofuran / 2 h / -78 °C

5: 99 percent / Dibal-H / CH₂Cl₂ / -78 °C

6: 93 percent / TiCl₄ / benzene / 0.5 h

7: 94 percent / TBAF / tetrahydrofuran

8: 89 percent / camphorsulfonic acid / benzene / 6 h / Heating

9: 73 percent / Dibal-H / CH₂Cl₂; hexane / 0 - 20 °C

With 1H-imidazole; camphor-10-sulfonic acid; tetrabutyl ammonium fluoride; titanium tetrachloride; diisobutylaluminium hydride; lithium hexamethyldisilazane; lithium diisopropyl amide; In tetrahydrofuran; 1,2-dimethoxyethane; hexane; dichloromethane; benzene;
DOI:10.1021/jo981083t

Reference yield:

: 123-11-5
4-methoxy-benzaldehyde

: 215317-78-5
(3R,5R)-5-[1,3]Dithian-2-yl-3-(4-methoxy-benzyloxy)-2,2-dimethyl-hexan-1-ol

Guidance literature:: Multi-step reaction with 2 steps

1: 89 percent / camphorsulfonic acid / benzene / 6 h / Heating

2: 73 percent / Dibal-H / CH₂Cl₂; hexane / 0 - 20 °C

With camphor-10-sulfonic acid; diisobutylaluminium hydride; In hexane; dichloromethane; benzene;
DOI:10.1021/jo981083t