Methanesulfonic acid (1S,2R)-2-benzyloxymethoxy-1-hydroxymethyl-propyl ester

Base Information

Chemical Name:Methanesulfonic acid (1S,2R)-2-benzyloxymethoxy-1-hydroxymethyl-propyl ester
CAS No.:155433-59-3
Molecular Formula:C₁₃H₂₀O₆S
Molecular Weight:304.364
Hs Code.:

Synonyms:Methanesulfonic acid (1S,2R)-2-benzyloxymethoxy-1-hydroxymethyl-propyl ester

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Chemical Property of Methanesulfonic acid (1S,2R)-2-benzyloxymethoxy-1-hydroxymethyl-propyl ester

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Technology Process of Methanesulfonic acid (1S,2R)-2-benzyloxymethoxy-1-hydroxymethyl-propyl ester

There total 4 articles about Methanesulfonic acid (1S,2R)-2-benzyloxymethoxy-1-hydroxymethyl-propyl ester 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: 96.0%

: 155433-43-5
2,2-Dimethyl-propionic acid (2S,3R)-3-benzyloxymethoxy-2-methanesulfonyloxy-butyl ester

: 155433-59-3
Methanesulfonic acid (1S,2R)-2-benzyloxymethoxy-1-hydroxymethyl-propyl ester

Guidance literature:: With diisobutylaluminium hydride; In dichloromethane; at -78 ℃; for 1h;
DOI:10.1016/S0040-4020(01)81547-7

Reference yield:

: 137531-95-4
(2S,3R)-3-benzyloxymethoxy-1,2-carbonyldioxybutane

: 155433-59-3
Methanesulfonic acid (1S,2R)-2-benzyloxymethoxy-1-hydroxymethyl-propyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 93 percent / K₂CO₃ / methanol / 10 h / Ambient temperature

2: triethylamine / 4-dimethylaminopyridine / CH₂Cl₂ / 10 h / Ambient temperature

3: triethylamine / 4-dimethylaminopyridine / CH₂Cl₂ / 1 h

4: 96 percent / diisobutyl aluminum hydride / CH₂Cl₂ / 1 h / -78 °C

With diisobutylaluminium hydride; potassium carbonate; triethylamine; dmap; In methanol; dichloromethane;
DOI:10.1016/S0040-4020(01)81547-7

Reference yield:

: 155433-45-7
(2S,3R)-3-benzyloxymethoxy-butane-1,2-diol

: 155433-59-3
Methanesulfonic acid (1S,2R)-2-benzyloxymethoxy-1-hydroxymethyl-propyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / 4-dimethylaminopyridine / CH₂Cl₂ / 10 h / Ambient temperature

2: triethylamine / 4-dimethylaminopyridine / CH₂Cl₂ / 1 h

3: 96 percent / diisobutyl aluminum hydride / CH₂Cl₂ / 1 h / -78 °C

With diisobutylaluminium hydride; triethylamine; dmap; In dichloromethane;
DOI:10.1016/S0040-4020(01)81547-7