(4R,5R)-5-((R)-2-Benzyloxy-1-hydroxymethyl-ethyl)-4-methoxy-oxazolidin-2-one

Base Information

Chemical Name:(4R,5R)-5-((R)-2-Benzyloxy-1-hydroxymethyl-ethyl)-4-methoxy-oxazolidin-2-one
CAS No.:214962-91-1
Molecular Formula:C₁₄H₁₉NO₅
Molecular Weight:281.309
Hs Code.:

Synonyms:(4R,5R)-5-((R)-2-Benzyloxy-1-hydroxymethyl-ethyl)-4-methoxy-oxazolidin-2-one

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Chemical Property of (4R,5R)-5-((R)-2-Benzyloxy-1-hydroxymethyl-ethyl)-4-methoxy-oxazolidin-2-one

Chemical Property:

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Technology Process of (4R,5R)-5-((R)-2-Benzyloxy-1-hydroxymethyl-ethyl)-4-methoxy-oxazolidin-2-one

There total 6 articles about (4R,5R)-5-((R)-2-Benzyloxy-1-hydroxymethyl-ethyl)-4-methoxy-oxazolidin-2-one 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: 82.0%

: C₂₆H₃₃NO₈

: 214962-91-1
(4R,5R)-5-((R)-2-Benzyloxy-1-hydroxymethyl-ethyl)-4-methoxy-oxazolidin-2-one

Guidance literature:: With methanol; lithium borohydride; In tetrahydrofuran; at 0 ℃;
DOI:10.1016/S0040-4039(98)01515-9

Reference yield:

: 3-benzyloxy-2,2-dichloropropionic acid

: 214962-91-1
(4R,5R)-5-((R)-2-Benzyloxy-1-hydroxymethyl-ethyl)-4-methoxy-oxazolidin-2-one

Guidance literature:: Multi-step reaction with 6 steps

3: 75 percent / RuCl₂(PPh₃)3 / benzene / 120 h / Heating

4: Heating

5: (TMS)3SiH, Et₃B / toluene / -78 °C

6: 82 percent / LiBH₄-MeOH / tetrahydrofuran / 0 °C

With methanol; lithium borohydride; tris(triphenylphosphine)ruthenium(II) chloride; triethyl borane; tris-(trimethylsilyl)silane; In tetrahydrofuran; toluene; benzene;
DOI:10.1016/S0040-4039(98)01515-9

Reference yield:

: (1R,2S,4S)-2-[2-(3-Benzyloxy-2,2-dichloro-propionyloxy)-ethoxy]-7,7-dimethyl-bicyclo[2.2.1]heptane-1-carboxylic acid

: 214962-91-1
(4R,5R)-5-((R)-2-Benzyloxy-1-hydroxymethyl-ethyl)-4-methoxy-oxazolidin-2-one

Guidance literature:: Multi-step reaction with 5 steps

2: 75 percent / RuCl₂(PPh₃)3 / benzene / 120 h / Heating

3: Heating

4: (TMS)3SiH, Et₃B / toluene / -78 °C

5: 82 percent / LiBH₄-MeOH / tetrahydrofuran / 0 °C

With methanol; lithium borohydride; tris(triphenylphosphine)ruthenium(II) chloride; triethyl borane; tris-(trimethylsilyl)silane; In tetrahydrofuran; toluene; benzene;
DOI:10.1016/S0040-4039(98)01515-9