(E)-ethyl 3-(((2R,3S)-3-(benzyloxy)-4-(1,3-dithian-2-yl)butan-2-yl)oxy)acrylate

Base Information

Chemical Name:(E)-ethyl 3-(((2R,3S)-3-(benzyloxy)-4-(1,3-dithian-2-yl)butan-2-yl)oxy)acrylate
CAS No.:1592771-03-3
Molecular Formula:C₂₀H₂₈O₄S₂
Molecular Weight:396.572
Hs Code.:

Synonyms:(E)-ethyl 3-(((2R,3S)-3-(benzyloxy)-4-(1,3-dithian-2-yl)butan-2-yl)oxy)acrylate

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Chemical Property of (E)-ethyl 3-(((2R,3S)-3-(benzyloxy)-4-(1,3-dithian-2-yl)butan-2-yl)oxy)acrylate

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Technology Process of (E)-ethyl 3-(((2R,3S)-3-(benzyloxy)-4-(1,3-dithian-2-yl)butan-2-yl)oxy)acrylate

There total 5 articles about (E)-ethyl 3-(((2R,3S)-3-(benzyloxy)-4-(1,3-dithian-2-yl)butan-2-yl)oxy)acrylate 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:

: methyl 3-O-benzyl-5-O-(p-toluenesulfonyl)-2-deoxy-D-ribofuranoside

: 1592771-03-3
(E)-ethyl 3-(((2R,3S)-3-(benzyloxy)-4-(1,3-dithian-2-yl)butan-2-yl)oxy)acrylate

Guidance literature:: Multi-step reaction with 3 steps

1: lithium triethylborohydride / tetrahydrofuran / 6.25 h / 20 - 45 °C / Inert atmosphere

2: boron trifluoride diethyl etherate / dichloromethane / 0.67 h / 0 - 20 °C / Inert atmosphere

3: 4-methyl-morpholine / dichloromethane / 2 h / 20 °C / Inert atmosphere

With 4-methyl-morpholine; boron trifluoride diethyl etherate; lithium triethylborohydride; In tetrahydrofuran; dichloromethane;
DOI:10.1021/ol500788c

Reference yield:

: methyl 3-O-benzyl-2,5-dideoxy-D-erythropentofuranoside

: 1592771-03-3
(E)-ethyl 3-(((2R,3S)-3-(benzyloxy)-4-(1,3-dithian-2-yl)butan-2-yl)oxy)acrylate

Guidance literature:: Multi-step reaction with 2 steps

1: boron trifluoride diethyl etherate / dichloromethane / 0.67 h / 0 - 20 °C / Inert atmosphere

2: 4-methyl-morpholine / dichloromethane / 2 h / 20 °C / Inert atmosphere

With 4-methyl-morpholine; boron trifluoride diethyl etherate; In dichloromethane;
DOI:10.1021/ol500788c

Reference yield:

: 10437-39-5
methyl 2-deoxy-5-O-(p-toluenesulfonyl)-α,β-D-erythro-pentofuranoside

: 1592771-03-3
(E)-ethyl 3-(((2R,3S)-3-(benzyloxy)-4-(1,3-dithian-2-yl)butan-2-yl)oxy)acrylate

Guidance literature:: Multi-step reaction with 4 steps

1: potassium tert-butylate / tetrahydrofuran / 0.75 h / 0 - 20 °C / Inert atmosphere

2: lithium triethylborohydride / tetrahydrofuran / 6.25 h / 20 - 45 °C / Inert atmosphere

3: boron trifluoride diethyl etherate / dichloromethane / 0.67 h / 0 - 20 °C / Inert atmosphere

4: 4-methyl-morpholine / dichloromethane / 2 h / 20 °C / Inert atmosphere

With 4-methyl-morpholine; boron trifluoride diethyl etherate; potassium tert-butylate; lithium triethylborohydride; In tetrahydrofuran; dichloromethane;
DOI:10.1021/ol500788c