1,5-anhydro-2-deoxy-3,4-di-O-benzyl-6-O-levulinoyl-D-arabino-hex-1-enitol

Base Information

Chemical Name:1,5-anhydro-2-deoxy-3,4-di-O-benzyl-6-O-levulinoyl-D-arabino-hex-1-enitol
CAS No.:373606-52-1
Molecular Formula:C₂₅H₂₈O₆
Molecular Weight:424.494
Hs Code.:

Synonyms:1,5-anhydro-2-deoxy-3,4-di-O-benzyl-6-O-levulinoyl-D-arabino-hex-1-enitol

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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 1,5-anhydro-2-deoxy-3,4-di-O-benzyl-6-O-levulinoyl-D-arabino-hex-1-enitol

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Technology Process of 1,5-anhydro-2-deoxy-3,4-di-O-benzyl-6-O-levulinoyl-D-arabino-hex-1-enitol

There total 3 articles about 1,5-anhydro-2-deoxy-3,4-di-O-benzyl-6-O-levulinoyl-D-arabino-hex-1-enitol 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:

: 137915-37-8
1,2-dideoxy-6-O-triisopropylsilyl-D-arabino-1-hexenopyranose

: 373606-52-1
1,5-anhydro-2-deoxy-3,4-di-O-benzyl-6-O-levulinoyl-D-arabino-hex-1-enitol

Guidance literature:: Multi-step reaction with 3 steps

1: 89 percent / NaH / dimethylformamide

2: TBAF / acetic acid

3: DIPC; DMAP

With dmap; bis-2-propyl carbonate; tetrabutyl ammonium fluoride; sodium hydride; In acetic acid; N,N-dimethyl-formamide;
DOI:10.1002/hlca.200390331

Reference yield:

: 196703-95-4
1,5-anhydro-2-deoxy-3,4-di-O-benzyl-6-O-triisopropylsilyl-D-arabino-hex-1-enitol

: 373606-52-1
1,5-anhydro-2-deoxy-3,4-di-O-benzyl-6-O-levulinoyl-D-arabino-hex-1-enitol

Guidance literature:: Multi-step reaction with 2 steps

1: TBAF / acetic acid

2: DIPC; DMAP

With dmap; bis-2-propyl carbonate; tetrabutyl ammonium fluoride; In acetic acid;
DOI:10.1002/hlca.200390331