Acetic acid (2R,3R,4R,5R,6S)-4-acetoxy-5-hydroxy-6-methoxy-2-trityloxymethyl-tetrahydro-pyran-3-yl ester

Base Information

Chemical Name:Acetic acid (2R,3R,4R,5R,6S)-4-acetoxy-5-hydroxy-6-methoxy-2-trityloxymethyl-tetrahydro-pyran-3-yl ester
CAS No.:53717-01-4
Molecular Formula:C₃₀H₃₂O₈
Molecular Weight:520.579
Hs Code.:

Synonyms:Acetic acid (2R,3R,4R,5R,6S)-4-acetoxy-5-hydroxy-6-methoxy-2-trityloxymethyl-tetrahydro-pyran-3-yl ester

Suppliers and Price of Acetic acid (2R,3R,4R,5R,6S)-4-acetoxy-5-hydroxy-6-methoxy-2-trityloxymethyl-tetrahydro-pyran-3-yl ester

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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 Acetic acid (2R,3R,4R,5R,6S)-4-acetoxy-5-hydroxy-6-methoxy-2-trityloxymethyl-tetrahydro-pyran-3-yl ester

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of Acetic acid (2R,3R,4R,5R,6S)-4-acetoxy-5-hydroxy-6-methoxy-2-trityloxymethyl-tetrahydro-pyran-3-yl ester

There total 2 articles about Acetic acid (2R,3R,4R,5R,6S)-4-acetoxy-5-hydroxy-6-methoxy-2-trityloxymethyl-tetrahydro-pyran-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:

: 7511-40-2,18031-49-7,31873-39-9,38982-56-8,63167-74-8,87591-35-3
methyl 2,3,4-tri-O-acetyl-6-O-trityl-α-D-glucopyranoside

: 53716-99-7
Acetic acid (2R,3S,4S,5R,6S)-5-acetoxy-4-hydroxy-6-methoxy-2-trityloxymethyl-tetrahydro-pyran-3-yl ester

: 53717-01-4
Acetic acid (2R,3R,4R,5R,6S)-4-acetoxy-5-hydroxy-6-methoxy-2-trityloxymethyl-tetrahydro-pyran-3-yl ester

Guidance literature:: With zirconocene dichloride; diisobutylaluminium hydride; In tetrahydrofuran; at -20 ℃; Overall yield = 76 %; Overall yield = 98 mg; regioselective reaction; Inert atmosphere;
DOI:10.1021/acs.orglett.8b03947