(R)-4-Benzyl-3-(6-benzyloxymethoxy-2-ethyl-hexanoyl)-oxazolidin-2-one

Base Information

• Chemical Name: (R)-4-Benzyl-3-(6-benzyloxymethoxy-2-ethyl-hexanoyl)-oxazolidin-2-one
• CAS No.: 128057-11-4
• Molecular Formula: C₂₆H₃₃NO₅
• Molecular Weight: 439.552
• Mol file: 128057-11-4.mol

Synonyms:(R)-4-Benzyl-3-(6-benzyloxymethoxy-2-ethyl-hexanoyl)-oxazolidin-2-one

Chemical Property of (R)-4-Benzyl-3-(6-benzyloxymethoxy-2-ethyl-hexanoyl)-oxazolidin-2-one

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (R)-4-Benzyl-3-(6-benzyloxymethoxy-2-ethyl-hexanoyl)-oxazolidin-2-one

There total 7 articles about (R)-4-Benzyl-3-(6-benzyloxymethoxy-2-ethyl-hexanoyl)-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: 28.0%

(R)-4-Benzyl-3-(6-benzyloxymethoxy-hexanoyl)-oxazolidin-2-one (128057-10-3) + ethyl iodide (75-03-6) → (R)-4-Benzyl-3-(6-benzyloxymethoxy-2-ethyl-hexanoyl)-oxazolidin-2-one (128057-11-4)

Guidance literature:

DOI:10.1021/jo00298a016

Reference yield:

Benzyloxymethyl chloride (3587-60-8) → (R)-4-Benzyl-3-(6-benzyloxymethoxy-2-ethyl-hexanoyl)-oxazolidin-2-one (128057-11-4)

Guidance literature:

Multi-step reaction with 4 steps

1: i-Pr₂NEt / CH₂Cl₂ / Ambient temperature

2: LiOH, aq. MeOH / tetrahydrofuran

3: 1) NEt₃ / 1) THF, 0 deg C

4: 1) NaN(TMS)2 / 1) THF, 2) -78 to -30 deg C

With methanol; lithium hydroxide; sodium hexamethyldisilazane; triethylamine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane;

DOI:10.1021/jo00298a016

Reference yield:

methyl 6-hydroxycaproate (4547-43-7) → (R)-4-Benzyl-3-(6-benzyloxymethoxy-2-ethyl-hexanoyl)-oxazolidin-2-one (128057-11-4)

Guidance literature:

Multi-step reaction with 4 steps

1: i-Pr₂NEt / CH₂Cl₂ / Ambient temperature

2: LiOH, aq. MeOH / tetrahydrofuran

3: 1) NEt₃ / 1) THF, 0 deg C

4: 1) NaN(TMS)2 / 1) THF, 2) -78 to -30 deg C

With methanol; lithium hydroxide; sodium hexamethyldisilazane; triethylamine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane;

DOI:10.1021/jo00298a016

upstream raw materials:

trifluoromethanesulfonic acid ethyl ester

(R)-4-Benzyl-3-(6-benzyloxymethoxy-hexanoyl)-oxazolidin-2-one

6-(((benzyloxy)methylene)oxy)-2-ethylhexanoic acid

(R)-4-benzyl-2-oxazolidinone lithium salt

Downstream raw materials:

(R)-6-Benzyloxymethoxy-2-ethyl-hexan-1-ol

(R)-5-(Toluene-4-sulfonylmethyl)-heptanal

1-((R)-6-Benzyloxymethoxy-2-ethyl-hexane-1-sulfonyl)-4-methyl-benzene

(2R,11R)-1-(tert-Butyl-dimethyl-silanyloxy)-2-methyl-11-(toluene-4-sulfonylmethyl)-tridecan-7-ol