4-Bromo-benzoic acid (2R,3R,4S,5R)-5-hydroxymethyl-5-methoxy-4-[(E)-3-(4-methoxy-phenyl)-acryloyloxy]-2-[(E)-3-(4-methoxy-phenyl)-acryloyloxymethyl]-tetrahydro-furan-3-yl ester

Base Information

Chemical Name:4-Bromo-benzoic acid (2R,3R,4S,5R)-5-hydroxymethyl-5-methoxy-4-[(E)-3-(4-methoxy-phenyl)-acryloyloxy]-2-[(E)-3-(4-methoxy-phenyl)-acryloyloxymethyl]-tetrahydro-furan-3-yl ester
CAS No.:147694-26-6
Molecular Formula:C₃₄H₃₃BrO₁₁
Molecular Weight:697.533
Hs Code.:

4-Bromo-benzoic acid (2R,3R,4S,5R)-5-hydroxymethyl-5-methoxy-4-[(E)-3-(4-methoxy-phenyl)-acryloyloxy]-2-[(E)-3-(4-methoxy-phenyl)-acryloyloxymethyl]-tetrahydro-furan-3-yl ester

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Chemical Property of 4-Bromo-benzoic acid (2R,3R,4S,5R)-5-hydroxymethyl-5-methoxy-4-[(E)-3-(4-methoxy-phenyl)-acryloyloxy]-2-[(E)-3-(4-methoxy-phenyl)-acryloyloxymethyl]-tetrahydro-furan-3-yl ester

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Technology Process of 4-Bromo-benzoic acid (2R,3R,4S,5R)-5-hydroxymethyl-5-methoxy-4-[(E)-3-(4-methoxy-phenyl)-acryloyloxy]-2-[(E)-3-(4-methoxy-phenyl)-acryloyloxymethyl]-tetrahydro-furan-3-yl ester

There total 8 articles about 4-Bromo-benzoic acid (2R,3R,4S,5R)-5-hydroxymethyl-5-methoxy-4-[(E)-3-(4-methoxy-phenyl)-acryloyloxy]-2-[(E)-3-(4-methoxy-phenyl)-acryloyloxymethyl]-tetrahydro-furan-3-yl 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:

: 943-89-5
(E)-3-(4-methoxyphenyl)acrylic acid

: 147694-26-6
4-Bromo-benzoic acid (2R,3R,4S,5R)-5-hydroxymethyl-5-methoxy-4-[(E)-3-(4-methoxy-phenyl)-acryloyloxy]-2-[(E)-3-(4-methoxy-phenyl)-acryloyloxymethyl]-tetrahydro-furan-3-yl ester

Guidance literature:: Multi-step reaction with 5 steps

1: thionyl chloride / benzene / 2 h / Heating

2: pyridine / Ambient temperature

3: pyridine / silver triflate, 4-dimethylaminopyridine / CH₂Cl₂

4: HF, pyridine / Ambient temperature

5: pyridine / Ambient temperature

With pyridine; thionyl chloride; hydrogen fluoride; dmap; silver trifluoromethanesulfonate; In dichloromethane; benzene;
DOI:10.1016/0008-6215(93)84200-P

Reference yield:

: 34446-64-5,42996-84-9
(E)-3-(4-methoxyphenyl)propenoyl chloride

: 147694-26-6
4-Bromo-benzoic acid (2R,3R,4S,5R)-5-hydroxymethyl-5-methoxy-4-[(E)-3-(4-methoxy-phenyl)-acryloyloxy]-2-[(E)-3-(4-methoxy-phenyl)-acryloyloxymethyl]-tetrahydro-furan-3-yl ester

Guidance literature:: Multi-step reaction with 4 steps

1: pyridine / Ambient temperature

2: pyridine / silver triflate, 4-dimethylaminopyridine / CH₂Cl₂

3: HF, pyridine / Ambient temperature

4: pyridine / Ambient temperature

With pyridine; hydrogen fluoride; dmap; silver trifluoromethanesulfonate; In dichloromethane;
DOI:10.1016/0008-6215(93)84200-P

Reference yield:

: 147694-17-5
(E)-3-(4-Methoxy-phenyl)-acrylic acid (2R,3S,4R,5R)-2,5-bis-(tert-butyl-dimethyl-silanyloxymethyl)-4-hydroxy-2-methoxy-tetrahydro-furan-3-yl ester

: 147694-26-6
4-Bromo-benzoic acid (2R,3R,4S,5R)-5-hydroxymethyl-5-methoxy-4-[(E)-3-(4-methoxy-phenyl)-acryloyloxy]-2-[(E)-3-(4-methoxy-phenyl)-acryloyloxymethyl]-tetrahydro-furan-3-yl ester

Guidance literature:: Multi-step reaction with 3 steps

1: pyridine / silver triflate, 4-dimethylaminopyridine / CH₂Cl₂

2: HF, pyridine / Ambient temperature

3: pyridine / Ambient temperature

With pyridine; hydrogen fluoride; dmap; silver trifluoromethanesulfonate; In dichloromethane;
DOI:10.1016/0008-6215(93)84200-P