Z-2,4-O-Benzylidene-1-O-tert-butyldimethylsilyl-5,6-dideoxy-6-C-(2,4-dichlorophenyl)-3-O-(p-tolylsulfonyl)-D-xylo-hex-5-enitol

Base Information

Chemical Name:Z-2,4-O-Benzylidene-1-O-tert-butyldimethylsilyl-5,6-dideoxy-6-C-(2,4-dichlorophenyl)-3-O-(p-tolylsulfonyl)-D-xylo-hex-5-enitol
CAS No.:141240-14-4
Molecular Formula:C₃₂H₃₈Cl₂O₆SSi
Molecular Weight:649.708
Hs Code.:

Synonyms:Z-2,4-O-Benzylidene-1-O-tert-butyldimethylsilyl-5,6-dideoxy-6-C-(2,4-dichlorophenyl)-3-O-(p-tolylsulfonyl)-D-xylo-hex-5-enitol

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Chemical Property of Z-2,4-O-Benzylidene-1-O-tert-butyldimethylsilyl-5,6-dideoxy-6-C-(2,4-dichlorophenyl)-3-O-(p-tolylsulfonyl)-D-xylo-hex-5-enitol

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Technology Process of Z-2,4-O-Benzylidene-1-O-tert-butyldimethylsilyl-5,6-dideoxy-6-C-(2,4-dichlorophenyl)-3-O-(p-tolylsulfonyl)-D-xylo-hex-5-enitol

There total 5 articles about Z-2,4-O-Benzylidene-1-O-tert-butyldimethylsilyl-5,6-dideoxy-6-C-(2,4-dichlorophenyl)-3-O-(p-tolylsulfonyl)-D-xylo-hex-5-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: 100.0%

: 141240-12-2
Z-2,4-O-Benzylidene-1-O-tert-butyl-dimethylsilyl-5,6-dideoxy-6-C-(2,4-dichlorophenyl)-D-xylo-hex-5-enitol

: 98-59-9
p-toluenesulfonyl chloride

: 141240-14-4
Z-2,4-O-Benzylidene-1-O-tert-butyldimethylsilyl-5,6-dideoxy-6-C-(2,4-dichlorophenyl)-3-O-(p-tolylsulfonyl)-D-xylo-hex-5-enitol

Guidance literature:: With pyridine; for 36h;
DOI:10.1016/S0008-6215(00)90499-3

Reference yield:

: 18162-48-6
tert-butyldimethylsilyl chloride

: 141240-14-4
Z-2,4-O-Benzylidene-1-O-tert-butyldimethylsilyl-5,6-dideoxy-6-C-(2,4-dichlorophenyl)-3-O-(p-tolylsulfonyl)-D-xylo-hex-5-enitol

Guidance literature:: Multi-step reaction with 2 steps

1: 89.4 percent / imidazole / dimethylformamide / 0.75 h / Ambient temperature

2: 100 percent / pyridine / 36 h

With pyridine; 1H-imidazole; In N,N-dimethyl-formamide;
DOI:10.1016/S0008-6215(00)90499-3

Reference yield:

: 141240-15-5
(Z)-2,4-O-Benzylidene-1-O-tert-butyldimethylsilyl-5,6-dideoxy-6-C-(2,4-dichlorophenyl)-3-O-(4-nitrobenzoyl)-D-xylo-hex-5-enitol

: 141240-14-4
Z-2,4-O-Benzylidene-1-O-tert-butyldimethylsilyl-5,6-dideoxy-6-C-(2,4-dichlorophenyl)-3-O-(p-tolylsulfonyl)-D-xylo-hex-5-enitol

Guidance literature:: Multi-step reaction with 3 steps

1: 77 percent / 1M H₂SO₄ / methanol / 0.75 h

2: 89.4 percent / imidazole / dimethylformamide / 0.75 h / Ambient temperature

3: 100 percent / pyridine / 36 h

With pyridine; 1H-imidazole; sulfuric acid; In methanol; N,N-dimethyl-formamide;
DOI:10.1016/S0008-6215(00)90499-3