(2R,3S,4S)-3,4-Bis-benzyloxy-2-benzyloxymethyl-tetrahydro-thiophene 1-oxide

Base Information

Chemical Name:(2R,3S,4S)-3,4-Bis-benzyloxy-2-benzyloxymethyl-tetrahydro-thiophene 1-oxide
CAS No.:187590-79-0
Molecular Formula:C₂₆H₂₈O₄S
Molecular Weight:436.572
Hs Code.:

Synonyms:(2R,3S,4S)-3,4-Bis-benzyloxy-2-benzyloxymethyl-tetrahydro-thiophene 1-oxide

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

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Chemical Property of (2R,3S,4S)-3,4-Bis-benzyloxy-2-benzyloxymethyl-tetrahydro-thiophene 1-oxide

Chemical Property:

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Technology Process of (2R,3S,4S)-3,4-Bis-benzyloxy-2-benzyloxymethyl-tetrahydro-thiophene 1-oxide

There total 3 articles about (2R,3S,4S)-3,4-Bis-benzyloxy-2-benzyloxymethyl-tetrahydro-thiophene 1-oxide 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:

: 187590-77-8
1,4-anhydro-2,3,5-tri-O-benzyl-4-thio-D-arabinitol

: 187590-79-0
(2R,3S,4S)-3,4-Bis-benzyloxy-2-benzyloxymethyl-tetrahydro-thiophene 1-oxide

Guidance literature:: With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at -78 ℃; for 0.5h;
DOI:10.1021/jm9701536

Reference yield:

: 100-44-7
benzyl chloride

: 187590-79-0
(2R,3S,4S)-3,4-Bis-benzyloxy-2-benzyloxymethyl-tetrahydro-thiophene 1-oxide

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) NaH / 1.) DMF, 0 deg C, 1 h, 2.) DMF, RT, overnight

2: m-CPBA / CH₂Cl₂ / 0.5 h / -78 °C

With sodium hydride; 3-chloro-benzenecarboperoxoic acid; In dichloromethane;
DOI:10.1021/jm9701536

Reference yield:

: 160882-25-7
3-O-benzyl-1-deoxy-4-thio-D-arabino-furanose

: 187590-79-0
(2R,3S,4S)-3,4-Bis-benzyloxy-2-benzyloxymethyl-tetrahydro-thiophene 1-oxide

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) NaH / 1.) DMF, 0 deg C, 1 h, 2.) DMF, RT, overnight

2: m-CPBA / CH₂Cl₂ / 0.5 h / -78 °C

With sodium hydride; 3-chloro-benzenecarboperoxoic acid; In dichloromethane;
DOI:10.1021/jm9701536