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

Base Information

Chemical Name:(E)-3-[(2S,3S)-3-((1S,2R)-4-Benzyloxy-2-hydroxy-1-methyl-butyl)-oxiranyl]-2-methyl-acrylic acid ethyl ester
CAS No.:851592-65-9
Molecular Formula:C₂₀H₂₈O₅
Molecular Weight:348.439
Hs Code.:

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

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

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

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

: 851592-82-0
(E)-3-[(2S,3S)-3-((1R,2R)-4-Benzyloxy-1-methyl-2-triethylsilanyloxy-butyl)-oxiranyl]-2-methyl-acrylic acid ethyl ester

: 851592-65-9
(E)-3-[(2S,3S)-3-((1S,2R)-4-Benzyloxy-2-hydroxy-1-methyl-butyl)-oxiranyl]-2-methyl-acrylic acid ethyl ester

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 0 ℃;
DOI:10.1002/anie.200462300

Reference yield:

: (2R,3R)-3-(2-Benzyloxy-ethyl)-oxirane-2-carbaldehyde

: 851592-65-9
(E)-3-[(2S,3S)-3-((1S,2R)-4-Benzyloxy-2-hydroxy-1-methyl-butyl)-oxiranyl]-2-methyl-acrylic acid ethyl ester

Guidance literature:: Multi-step reaction with 8 steps

1: NaH / tetrahydrofuran / 0 °C

2: 96 percent / D₂O; CH₂Cl₂ / -30 - -10 °C

3: imidazole; 4-(dimethylamino)pyridine / CH₂Cl₂ / 20 °C

4: diisobutylaluminum hydride / tetrahydrofuran / 0 °C

5: 88 percent / 3-chloroperoxybenzoic acid / CH₂Cl₂ / 0 °C

6: pyridinium dichromate; molecular sieves 4 Angstroem / 1,2-dichloro-ethane / 60 °C

7: 0 °C

8: tetrabutylammonium fluoride / tetrahydrofuran / 0 °C

With 1H-imidazole; dmap; dipyridinium dichromate; 4 A molecular sieve; tetrabutyl ammonium fluoride; sodium hydride; diisobutylaluminium hydride; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; dichloromethane; water-d2; 1,2-dichloro-ethane; 1: Horner-Wadsworth-Emmons reaction / 7: Wittig reaction;
DOI:10.1002/anie.200462300

Reference yield:

: 851592-61-5
(E)-3-[(2S,3R)-3-(2-Benzyloxy-ethyl)-oxiranyl]-acrylic acid ethyl ester

: 851592-65-9
(E)-3-[(2S,3S)-3-((1S,2R)-4-Benzyloxy-2-hydroxy-1-methyl-butyl)-oxiranyl]-2-methyl-acrylic acid ethyl ester

Guidance literature:: Multi-step reaction with 7 steps

1: 96 percent / D₂O; CH₂Cl₂ / -30 - -10 °C

2: imidazole; 4-(dimethylamino)pyridine / CH₂Cl₂ / 20 °C

3: diisobutylaluminum hydride / tetrahydrofuran / 0 °C

4: 88 percent / 3-chloroperoxybenzoic acid / CH₂Cl₂ / 0 °C

5: pyridinium dichromate; molecular sieves 4 Angstroem / 1,2-dichloro-ethane / 60 °C

6: 0 °C

7: tetrabutylammonium fluoride / tetrahydrofuran / 0 °C

With 1H-imidazole; dmap; dipyridinium dichromate; 4 A molecular sieve; tetrabutyl ammonium fluoride; diisobutylaluminium hydride; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; dichloromethane; water-d2; 1,2-dichloro-ethane; 6: Wittig reaction;
DOI:10.1002/anie.200462300