(4R,2R,3'S,4'S)-3-<5'-Benzyloxy-3'-(tert-butyldimethylsilyloxy)-2',4'-dimethylpentanoyl>-4-isopropyl-2-oxazolidinone

Base Information

Chemical Name:(4R,2R,3'S,4'S)-3-<5'-Benzyloxy-3'-(tert-butyldimethylsilyloxy)-2',4'-dimethylpentanoyl>-4-isopropyl-2-oxazolidinone
CAS No.:100649-10-3
Molecular Formula:C₂₆H₄₃NO₅Si
Molecular Weight:477.717
Hs Code.:

Synonyms:(4R,2R,3'S,4'S)-3-<5'-Benzyloxy-3'-(tert-butyldimethylsilyloxy)-2',4'-dimethylpentanoyl>-4-isopropyl-2-oxazolidinone

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Chemical Property of (4R,2R,3'S,4'S)-3-<5'-Benzyloxy-3'-(tert-butyldimethylsilyloxy)-2',4'-dimethylpentanoyl>-4-isopropyl-2-oxazolidinone

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Technology Process of (4R,2R,3'S,4'S)-3-<5'-Benzyloxy-3'-(tert-butyldimethylsilyloxy)-2',4'-dimethylpentanoyl>-4-isopropyl-2-oxazolidinone

There total 3 articles about (4R,2R,3'S,4'S)-3-<5'-Benzyloxy-3'-(tert-butyldimethylsilyloxy)-2',4'-dimethylpentanoyl>-4-isopropyl-2-oxazolidinone 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: 100.0%

: 69739-34-0
t-butyldimethylsiyl triflate

: 97747-36-9
(4R,2'R,3'S,4'S)-3-(5'-Benzyloxy-3'-hydroxy-2',4'-dimethylpentanoyl)-4-isopropyl-2-oxazolidinone

: 100649-10-3
(4R,2R,3'S,4'S)-3-<5'-Benzyloxy-3'-(tert-butyldimethylsilyloxy)-2',4'-dimethylpentanoyl>-4-isopropyl-2-oxazolidinone

Guidance literature:: With 2,6-dimethylpyridine; In dichloromethane; for 1.5h; Ambient temperature;
DOI:10.1002/jlac.198519851203

Reference yield:

: 63930-49-4
(R)-3-(benzyloxy)-2-methylpropan-1-ol

: 100649-10-3
(4R,2R,3'S,4'S)-3-<5'-Benzyloxy-3'-(tert-butyldimethylsilyloxy)-2',4'-dimethylpentanoyl>-4-isopropyl-2-oxazolidinone

Guidance literature:: Multi-step reaction with 3 steps

1: DMSO, oxalyl chloride / CH₂Cl₂ / 0.25 h / -65 °C

3: 100 percent / 2,6-lutidine / CH₂Cl₂ / 1.5 h / Ambient temperature

With 2,6-dimethylpyridine; oxalyl dichloride; dimethyl sulfoxide; In dichloromethane;
DOI:10.1002/jlac.198519851203

Reference yield:

: 79027-28-4
(2S)-3-(benzyloxy)-2-methylpropanal

: 100649-10-3
(4R,2R,3'S,4'S)-3-<5'-Benzyloxy-3'-(tert-butyldimethylsilyloxy)-2',4'-dimethylpentanoyl>-4-isopropyl-2-oxazolidinone

Guidance literature:: Multi-step reaction with 2 steps

2: 100 percent / 2,6-lutidine / CH₂Cl₂ / 1.5 h / Ambient temperature

With 2,6-dimethylpyridine; In dichloromethane;
DOI:10.1002/jlac.198519851203