(E)-3-[(2R,3R)-3-((1S,2S,3S)-4-Benzyloxy-2-hydroxy-1,3-dimethyl-butyl)-oxiranyl]-acrylic acid ethyl ester

Base Information

Chemical Name:(E)-3-[(2R,3R)-3-((1S,2S,3S)-4-Benzyloxy-2-hydroxy-1,3-dimethyl-butyl)-oxiranyl]-acrylic acid ethyl ester
CAS No.:260433-39-4
Molecular Formula:C₂₀H₂₈O₅
Molecular Weight:348.439
Hs Code.:

Synonyms:(E)-3-[(2R,3R)-3-((1S,2S,3S)-4-Benzyloxy-2-hydroxy-1,3-dimethyl-butyl)-oxiranyl]-acrylic acid ethyl ester

Suppliers and Price of (E)-3-[(2R,3R)-3-((1S,2S,3S)-4-Benzyloxy-2-hydroxy-1,3-dimethyl-butyl)-oxiranyl]-acrylic acid ethyl ester

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of (E)-3-[(2R,3R)-3-((1S,2S,3S)-4-Benzyloxy-2-hydroxy-1,3-dimethyl-butyl)-oxiranyl]-acrylic acid ethyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (E)-3-[(2R,3R)-3-((1S,2S,3S)-4-Benzyloxy-2-hydroxy-1,3-dimethyl-butyl)-oxiranyl]-acrylic acid ethyl ester

There total 9 articles about (E)-3-[(2R,3R)-3-((1S,2S,3S)-4-Benzyloxy-2-hydroxy-1,3-dimethyl-butyl)-oxiranyl]-acrylic acid ethyl 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:

: 260433-38-3
(E)-3-[(2R,3R)-3-((1R,2S,3S)-4-Benzyloxy-1,3-dimethyl-2-triethylsilanyloxy-butyl)-oxiranyl]-acrylic acid ethyl ester

: 260433-39-4
(E)-3-[(2R,3R)-3-((1S,2S,3S)-4-Benzyloxy-2-hydroxy-1,3-dimethyl-butyl)-oxiranyl]-acrylic acid ethyl ester

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran;
DOI:10.1039/a908342a

Reference yield:

: 81520-04-9
(2S,3S,4S)-5-(benzyloxy)-2,3-epoxy-4-methyl-1-pentanol

: 260433-39-4
(E)-3-[(2R,3R)-3-((1S,2S,3S)-4-Benzyloxy-2-hydroxy-1,3-dimethyl-butyl)-oxiranyl]-acrylic acid ethyl ester

Guidance literature:: Multi-step reaction with 9 steps

1.1: (COCl)2; DMSO; Et₃N / CH₂Cl₂ / -78 °C

2.1: NaH / tetrahydrofuran / 0 °C

2.2: tetrahydrofuran / 0 °C

3.1: 92 percent / H₂O / CH₂Cl₂ / -30 °C

4.1: imidazole; DMAP / CH₂Cl₂

5.1: DIBAL-H / tetrahydrofuran / 0 °C

6.1: MCPBA / CH₂Cl₂ / 0 °C

7.1: (COCl₂)2; DMSO; Et₃N / CH₂Cl₂ / -78 °C

8.1: NaH / tetrahydrofuran / 0 °C

8.2: tetrahydrofuran / 0 °C

9.1: Bu₄NF / tetrahydrofuran

With 1H-imidazole; dmap; oxalyl dichloride; (COCl₂)2; tetrabutyl ammonium fluoride; water; sodium hydride; diisobutylaluminium hydride; dimethyl sulfoxide; triethylamine; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; dichloromethane; 1.1: Oxidation / 2.1: Metallation / 2.2: Condensation / 3.1: Methylation / 4.1: Etherification / 5.1: Reduction / 6.1: Epoxidation / 7.1: Oxidation / 8.1: Metallation / 8.2: Condensation / 9.1: Substitution;
DOI:10.1039/a908342a

Reference yield:

: 136881-05-5
(E)-3-[(2S,3S)-3-((S)-2-Benzyloxy-1-methyl-ethyl)-oxiranyl]-acrylic acid ethyl ester

: 260433-39-4
(E)-3-[(2R,3R)-3-((1S,2S,3S)-4-Benzyloxy-2-hydroxy-1,3-dimethyl-butyl)-oxiranyl]-acrylic acid ethyl ester

Guidance literature:: Multi-step reaction with 7 steps

1.1: 92 percent / H₂O / CH₂Cl₂ / -30 °C

2.1: imidazole; DMAP / CH₂Cl₂

3.1: DIBAL-H / tetrahydrofuran / 0 °C

4.1: MCPBA / CH₂Cl₂ / 0 °C

5.1: (COCl₂)2; DMSO; Et₃N / CH₂Cl₂ / -78 °C

6.1: NaH / tetrahydrofuran / 0 °C

6.2: tetrahydrofuran / 0 °C

7.1: Bu₄NF / tetrahydrofuran

With 1H-imidazole; dmap; (COCl₂)2; tetrabutyl ammonium fluoride; water; sodium hydride; diisobutylaluminium hydride; dimethyl sulfoxide; triethylamine; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; dichloromethane; 1.1: Methylation / 2.1: Etherification / 3.1: Reduction / 4.1: Epoxidation / 5.1: Oxidation / 6.1: Metallation / 6.2: Condensation / 7.1: Substitution;
DOI:10.1039/a908342a