((2S,3S,4R,5R)-3,4,5-Tris-benzyloxy-tetrahydro-pyran-2-yl)-acetic acid ethyl ester

Base Information

Chemical Name:((2S,3S,4R,5R)-3,4,5-Tris-benzyloxy-tetrahydro-pyran-2-yl)-acetic acid ethyl ester
CAS No.:84781-70-4
Molecular Formula:C₃₀H₃₄O₆
Molecular Weight:490.596
Hs Code.:

Synonyms:((2S,3S,4R,5R)-3,4,5-Tris-benzyloxy-tetrahydro-pyran-2-yl)-acetic acid ethyl 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 ((2S,3S,4R,5R)-3,4,5-Tris-benzyloxy-tetrahydro-pyran-2-yl)-acetic acid ethyl ester

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Technology Process of ((2S,3S,4R,5R)-3,4,5-Tris-benzyloxy-tetrahydro-pyran-2-yl)-acetic acid ethyl ester

There total 1 articles about ((2S,3S,4R,5R)-3,4,5-Tris-benzyloxy-tetrahydro-pyran-2-yl)-acetic 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: 85.0%

: (Z)-(4S,5S,6R)-4,5,6-Tris-benzyloxy-7-hydroxy-hept-2-enoic acid ethyl ester

: 84781-70-4
((2S,3S,4R,5R)-3,4,5-Tris-benzyloxy-tetrahydro-pyran-2-yl)-acetic acid ethyl ester

Guidance literature:: With sodium ethanolate; In ethanol;
DOI:10.1002/hlca.19820650739

Reference yield: 90.0%

: 84781-70-4
((2S,3S,4R,5R)-3,4,5-Tris-benzyloxy-tetrahydro-pyran-2-yl)-acetic acid ethyl ester

: 84781-71-5
((2S,3S,4R,5R)-3,4,5-Tris-benzyloxy-tetrahydro-pyran-2-yl)-acetic acid

Guidance literature:: With hydroxide;
DOI:10.1002/hlca.19820650739

Reference yield:

: 84781-70-4
((2S,3S,4R,5R)-3,4,5-Tris-benzyloxy-tetrahydro-pyran-2-yl)-acetic acid ethyl ester

: 84781-72-6
1-((2S,3S,4R,5R)-3,4,5-Tris-benzyloxy-tetrahydro-pyran-2-yl)-propan-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: 90 percent / OH^(1-)

2: 50 percent

With hydroxide;
DOI:10.1002/hlca.19820650739