2-O-Benzoyl-4-brom-4-desoxy-3-O-methyl-D-threose-trimethylendithioacetal

Base Information

Chemical Name:2-O-Benzoyl-4-brom-4-desoxy-3-O-methyl-D-threose-trimethylendithioacetal
CAS No.:81577-89-1
Molecular Formula:C₁₅H₁₉BrO₃S₂
Molecular Weight:391.35
Hs Code.:

Synonyms:2-O-Benzoyl-4-brom-4-desoxy-3-O-methyl-D-threose-trimethylendithioacetal

Suppliers and Price of 2-O-Benzoyl-4-brom-4-desoxy-3-O-methyl-D-threose-trimethylendithioacetal

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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 2-O-Benzoyl-4-brom-4-desoxy-3-O-methyl-D-threose-trimethylendithioacetal

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Technology Process of 2-O-Benzoyl-4-brom-4-desoxy-3-O-methyl-D-threose-trimethylendithioacetal

There total 3 articles about 2-O-Benzoyl-4-brom-4-desoxy-3-O-methyl-D-threose-trimethylendithioacetal 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: 86.0%

: 109-80-8
1.3-propanedithiol

: 81577-76-6
2-O-Benzoyl-4-brom-4-desoxy-3-O-methyl-D-threose-dimethylacetal

: 81577-89-1
2-O-Benzoyl-4-brom-4-desoxy-3-O-methyl-D-threose-trimethylendithioacetal

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; for 0.75h;

Reference yield: 77.0%

: 109-80-8
1.3-propanedithiol

: 81577-88-0
2-O-Benzoyl-4-brom-4-desoxy-3-O-methyl-D-threose

: 81577-89-1
2-O-Benzoyl-4-brom-4-desoxy-3-O-methyl-D-threose-trimethylendithioacetal

Guidance literature:: With hydrogenchloride; for 2h; Ambient temperature;

Reference yield:

: 81577-80-2
2-O-Benzoyl-4-brom-4-desoxy-3-O-methyl-D-threonsaeure-methylester

: 81577-89-1
2-O-Benzoyl-4-brom-4-desoxy-3-O-methyl-D-threose-trimethylendithioacetal

Guidance literature:: Multi-step reaction with 2 steps

1: 4 percent / 1.0M diisobutylaluminiumhydride / toluene; hexane / 1.08 h / -75 °C

2: 77 percent / conc. HCl / 2 h / Ambient temperature

With hydrogenchloride; diisobutylaluminium hydride; In hexane; toluene;