Benzoic acid (1R,2S,3S)-2-benzyl-3-hydroxy-4-(toluene-4-sulfonyloxy)-1-vinyl-butyl ester

Base Information

Chemical Name:Benzoic acid (1R,2S,3S)-2-benzyl-3-hydroxy-4-(toluene-4-sulfonyloxy)-1-vinyl-butyl ester
CAS No.:453547-55-2
Molecular Formula:C₂₇H₂₈O₆S
Molecular Weight:480.582
Hs Code.:

Synonyms:Benzoic acid (1R,2S,3S)-2-benzyl-3-hydroxy-4-(toluene-4-sulfonyloxy)-1-vinyl-butyl ester

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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 Benzoic acid (1R,2S,3S)-2-benzyl-3-hydroxy-4-(toluene-4-sulfonyloxy)-1-vinyl-butyl ester

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Technology Process of Benzoic acid (1R,2S,3S)-2-benzyl-3-hydroxy-4-(toluene-4-sulfonyloxy)-1-vinyl-butyl ester

There total 2 articles about Benzoic acid (1R,2S,3S)-2-benzyl-3-hydroxy-4-(toluene-4-sulfonyloxy)-1-vinyl-butyl ester 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:

: 453547-51-8
methyl 4-O-benzoyl-3-benzyl-6-bromo-3,6-dideoxy-α-D-altropyranoside

: 453547-55-2
Benzoic acid (1R,2S,3S)-2-benzyl-3-hydroxy-4-(toluene-4-sulfonyloxy)-1-vinyl-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 75 percent / zinc; sodium cyanoborohydride / H₂O; propan-1-ol / 0.83 h / 95 °C

2: 82 percent / triethylamine; N,N-dimethylpyridin-4-amine / CH₂Cl₂ / 4 h / 20 °C

With dmap; sodium cyanoborohydride; triethylamine; zinc; In propan-1-ol; dichloromethane; water;
DOI:10.1016/j.tet.2005.08.116

Reference yield:

: 453547-49-4
methyl 3-C-benzyl-4,6-O-benzylidene-3-deoxy-α-D-altropyranoside

: 453547-55-2
Benzoic acid (1R,2S,3S)-2-benzyl-3-hydroxy-4-(toluene-4-sulfonyloxy)-1-vinyl-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 85 percent / N-bromosuccinimide; BaCO₃ / CCl₄ / 0.67 h / Heating

2: 75 percent / zinc; sodium cyanoborohydride / H₂O; propan-1-ol / 0.83 h / 95 °C

3: 82 percent / triethylamine; N,N-dimethylpyridin-4-amine / CH₂Cl₂ / 4 h / 20 °C

With dmap; N-Bromosuccinimide; sodium cyanoborohydride; triethylamine; barium carbonate; zinc; In propan-1-ol; tetrachloromethane; dichloromethane; water;
DOI:10.1016/j.tet.2005.08.116

Reference yield: 86.0%

: 453547-55-2
Benzoic acid (1R,2S,3S)-2-benzyl-3-hydroxy-4-(toluene-4-sulfonyloxy)-1-vinyl-butyl ester

: 453547-57-4
Benzoic acid (R)-1-((R)-1-(S)-oxiranyl-2-phenyl-ethyl)-allyl ester

Guidance literature:: With lithium hexamethyldisilazane; In tetrahydrofuran; hexane; at -78 - 20 ℃; for 1.08333h;
DOI:10.1016/j.tet.2005.08.116