(4R,5S)-4,5-Bis-benzyloxymethyl-tetrahydro-thiophene-2-carboxylic acid ethyl ester

Base Information

Chemical Name:(4R,5S)-4,5-Bis-benzyloxymethyl-tetrahydro-thiophene-2-carboxylic acid ethyl ester
CAS No.:224581-37-7
Molecular Formula:C₂₃H₂₈O₄S
Molecular Weight:400.539
Hs Code.:

Synonyms:(4R,5S)-4,5-Bis-benzyloxymethyl-tetrahydro-thiophene-2-carboxylic acid ethyl ester

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Chemical Property of (4R,5S)-4,5-Bis-benzyloxymethyl-tetrahydro-thiophene-2-carboxylic acid ethyl ester

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Technology Process of (4R,5S)-4,5-Bis-benzyloxymethyl-tetrahydro-thiophene-2-carboxylic acid ethyl ester

There total 8 articles about (4R,5S)-4,5-Bis-benzyloxymethyl-tetrahydro-thiophene-2-carboxylic 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: 90.0%

: 224581-35-5
((1S,2S)-1,2-Bis-benzyloxymethyl-3-methanesulfonyloxy-propylsulfanyl)-acetic acid ethyl ester

: 224581-37-7
(4R,5S)-4,5-Bis-benzyloxymethyl-tetrahydro-thiophene-2-carboxylic acid ethyl ester

Guidance literature:: With sodium hydride; In N,N-dimethyl-formamide; for 4h; Ambient temperature;
DOI:10.1016/S0960-894X(99)00142-0

Reference yield:

: 68973-05-7
(2R*,3S*)-2,3-bis((benzyloxy)methyl)oxirane

: 224581-37-7
(4R,5S)-4,5-Bis-benzyloxymethyl-tetrahydro-thiophene-2-carboxylic acid ethyl ester

Guidance literature:: Multi-step reaction with 8 steps

1: CuI / tetrahydrofuran; diethyl ether / 3.5 h / -25 °C

2: 30 percent aq. H₂O₂, NaHCO₃ / methanol; tetrahydrofuran / 8 h / 65 °C

3: 92 percent / imidazole / dimethylformamide / 7 h / Ambient temperature

4: 95 percent / Et₃N / 3 h / Ambient temperature

5: 97 percent / NaH / tetrahydrofuran / 2 h / Heating

6: 87 percent / n-Bu₄NF / tetrahydrofuran / 3 h / Ambient temperature

7: 86 percent / Et₃N / 3 h / Ambient temperature

8: 90 percent / NaH / dimethylformamide / 4 h / Ambient temperature

With 1H-imidazole; copper(l) iodide; tetrabutyl ammonium fluoride; dihydrogen peroxide; sodium hydride; sodium hydrogencarbonate; triethylamine; In tetrahydrofuran; methanol; diethyl ether; N,N-dimethyl-formamide;
DOI:10.1016/S0960-894X(99)00142-0

Reference yield:

: 224581-29-7
(2R,3R)-4-Benzyloxy-2-benzyloxymethyl-butane-1,3-diol

: 224581-37-7
(4R,5S)-4,5-Bis-benzyloxymethyl-tetrahydro-thiophene-2-carboxylic acid ethyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: 92 percent / imidazole / dimethylformamide / 7 h / Ambient temperature

2: 95 percent / Et₃N / 3 h / Ambient temperature

3: 97 percent / NaH / tetrahydrofuran / 2 h / Heating

4: 87 percent / n-Bu₄NF / tetrahydrofuran / 3 h / Ambient temperature

5: 86 percent / Et₃N / 3 h / Ambient temperature

6: 90 percent / NaH / dimethylformamide / 4 h / Ambient temperature

With 1H-imidazole; tetrabutyl ammonium fluoride; sodium hydride; triethylamine; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1016/S0960-894X(99)00142-0