(E)-3-[(2R,4S,5R)-4-((R)-1-Benzyloxy-2-[1,3]dithian-2-yl-ethyl)-2-phenyl-[1,3]dioxan-5-yloxy]-acrylic acid methyl ester

Base Information

Chemical Name:(E)-3-[(2R,4S,5R)-4-((R)-1-Benzyloxy-2-[1,3]dithian-2-yl-ethyl)-2-phenyl-[1,3]dioxan-5-yloxy]-acrylic acid methyl ester
CAS No.:669003-32-1
Molecular Formula:C₂₇H₃₂O₆S₂
Molecular Weight:516.679
Hs Code.:

Synonyms:(E)-3-[(2R,4S,5R)-4-((R)-1-Benzyloxy-2-[1,3]dithian-2-yl-ethyl)-2-phenyl-[1,3]dioxan-5-yloxy]-acrylic acid methyl ester

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Chemical Property of (E)-3-[(2R,4S,5R)-4-((R)-1-Benzyloxy-2-[1,3]dithian-2-yl-ethyl)-2-phenyl-[1,3]dioxan-5-yloxy]-acrylic acid methyl ester

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Technology Process of (E)-3-[(2R,4S,5R)-4-((R)-1-Benzyloxy-2-[1,3]dithian-2-yl-ethyl)-2-phenyl-[1,3]dioxan-5-yloxy]-acrylic acid methyl ester

There total 4 articles about (E)-3-[(2R,4S,5R)-4-((R)-1-Benzyloxy-2-[1,3]dithian-2-yl-ethyl)-2-phenyl-[1,3]dioxan-5-yloxy]-acrylic acid methyl 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: 97.0%

: 922-67-8
propynoic acid methyl ester

: 342901-70-6
(2R,4R,5R)-4-((R)-1-Benzyloxy-2-[1,3]dithian-2-yl-ethyl)-2-phenyl-[1,3]dioxan-5-ol

: 669003-32-1
(E)-3-[(2R,4S,5R)-4-((R)-1-Benzyloxy-2-[1,3]dithian-2-yl-ethyl)-2-phenyl-[1,3]dioxan-5-yloxy]-acrylic acid methyl ester

Guidance literature:: With 4-methyl-morpholine; In dichloromethane; at 20 ℃;
DOI:10.1002/1521-3773(20010316)40:6<1090::AID-ANIE10900>3.0.CO;2-W

Reference yield:

: 100-39-0
benzyl bromide

: 669003-32-1
(E)-3-[(2R,4S,5R)-4-((R)-1-Benzyloxy-2-[1,3]dithian-2-yl-ethyl)-2-phenyl-[1,3]dioxan-5-yloxy]-acrylic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: n-Bu₂SnO / benzene / Heating

1.2: CsF / dimethylformamide / 20 °C

2.1: NaH; CS₂; MeI / tetrahydrofuran / 20 °C

2.2: n-Bu₃SnH; AIBN / benzene / Heating

3.1: conc. HCl / CHCl₃ / 20 °C

3.2: 46 percent / camphorsulfonic acid / CH₂Cl₂ / 20 °C

4.1: 97 percent / N-methylmorpholine / CH₂Cl₂ / 20 °C

With 4-methyl-morpholine; hydrogenchloride; carbon disulfide; sodium hydride; di(n-butyl)tin oxide; methyl iodide; In tetrahydrofuran; dichloromethane; chloroform; benzene;
DOI:10.1002/1521-3773(20010316)40:6<1090::AID-ANIE10900>3.0.CO;2-W

Reference yield:

: 2774-19-8,14419-69-3,15887-67-9,23392-28-1,57539-08-9,61277-63-2,74410-51-8,76419-48-2,80734-73-2,86363-44-2,89301-79-1,94061-92-4,94062-87-0,108739-92-0,129706-93-0,143005-12-3,65877-21-6
(2R,4aR,6S,7S,8R,8aR)-8-Benzyloxy-6-methoxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-ol

: 669003-32-1
(E)-3-[(2R,4S,5R)-4-((R)-1-Benzyloxy-2-[1,3]dithian-2-yl-ethyl)-2-phenyl-[1,3]dioxan-5-yloxy]-acrylic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: NaH; CS₂; MeI / tetrahydrofuran / 20 °C

1.2: n-Bu₃SnH; AIBN / benzene / Heating

2.1: conc. HCl / CHCl₃ / 20 °C

2.2: 46 percent / camphorsulfonic acid / CH₂Cl₂ / 20 °C

3.1: 97 percent / N-methylmorpholine / CH₂Cl₂ / 20 °C

With 4-methyl-morpholine; hydrogenchloride; carbon disulfide; sodium hydride; methyl iodide; In tetrahydrofuran; dichloromethane; chloroform;
DOI:10.1002/1521-3773(20010316)40:6<1090::AID-ANIE10900>3.0.CO;2-W