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

Base Information

Chemical Name:(4R)-4-((2R)-5-m-dithian-2-ylpropyl)-2-(p-methoxyphenyl)-5,5-dimethyl-m-dioxane
CAS No.:215317-77-4
Molecular Formula:C₂₀H₃₀O₃S₂
Molecular Weight:382.588
Hs Code.:

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

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

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Technology Process of (4R)-4-((2R)-5-m-dithian-2-ylpropyl)-2-(p-methoxyphenyl)-5,5-dimethyl-m-dioxane

There total 8 articles about (4R)-4-((2R)-5-m-dithian-2-ylpropyl)-2-(p-methoxyphenyl)-5,5-dimethyl-m-dioxane 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: 89.0%

: 123-11-5
4-methoxy-benzaldehyde

: 215317-76-3
(3R,5R)-5-m-dithian-2-yl-2,2-dimethyl-1,3-hexanediol

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

Guidance literature:: With camphor-10-sulfonic acid; In benzene; for 6h; Heating;
DOI:10.1021/jo981083t

Reference yield:

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

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

Guidance literature:: Multi-step reaction with 8 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

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:

: 215317-59-2
tert-Butyl-((S)-2-methyl-2-oxiranyl-propoxy)-diphenyl-silane

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

Guidance literature:: Multi-step reaction with 7 steps

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

2: 81 percent / LiHMDS / tetrahydrofuran / -78 °C

3: 96 percent / LDA / tetrahydrofuran / 2 h / -78 °C

4: 99 percent / Dibal-H / CH₂Cl₂ / -78 °C

5: 93 percent / TiCl₄ / benzene / 0.5 h

6: 94 percent / TBAF / tetrahydrofuran

7: 89 percent / camphorsulfonic acid / benzene / 6 h / Heating

With 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