(2-hydroxy-ethyl) 2,3-di-O-benzyl-4-O-(tert-butoxycarbonylmethyl)-α-D-xylopyranoside

Base Information

Chemical Name:(2-hydroxy-ethyl) 2,3-di-O-benzyl-4-O-(tert-butoxycarbonylmethyl)-α-D-xylopyranoside
CAS No.:334536-13-9
Molecular Formula:C₂₇H₃₆O₈
Molecular Weight:488.578
Hs Code.:

Synonyms:(2-hydroxy-ethyl) 2,3-di-O-benzyl-4-O-(tert-butoxycarbonylmethyl)-α-D-xylopyranoside

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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 (2-hydroxy-ethyl) 2,3-di-O-benzyl-4-O-(tert-butoxycarbonylmethyl)-α-D-xylopyranoside

Chemical Property:

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Technology Process of (2-hydroxy-ethyl) 2,3-di-O-benzyl-4-O-(tert-butoxycarbonylmethyl)-α-D-xylopyranoside

There total 4 articles about (2-hydroxy-ethyl) 2,3-di-O-benzyl-4-O-(tert-butoxycarbonylmethyl)-α-D-xylopyranoside 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:

: 5292-43-3
bromoacetic acid tert-butyl ester

: 334536-13-9
(2-hydroxy-ethyl) 2,3-di-O-benzyl-4-O-(tert-butoxycarbonylmethyl)-α-D-xylopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 97 percent / NaH / dimethylformamide / 16 h

2: 98 percent / O₃; NaBH₄ / methanol; tetrahydrofuran

With sodium tetrahydroborate; sodium hydride; ozone; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; 1: etherification / 2: ozonolysis; reduction;
DOI:10.1016/S0968-0896(00)00256-X

Reference yield:

: 100-39-0
benzyl bromide

: 334536-13-9
(2-hydroxy-ethyl) 2,3-di-O-benzyl-4-O-(tert-butoxycarbonylmethyl)-α-D-xylopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: NaH / dimethylformamide / 16 h / 20 °C

2: 97 percent / NaH / dimethylformamide / 16 h

3: 98 percent / O₃; NaBH₄ / methanol; tetrahydrofuran

With sodium tetrahydroborate; sodium hydride; ozone; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; 1: etherification / 2: etherification / 3: ozonolysis; reduction;
DOI:10.1016/S0968-0896(00)00256-X

Reference yield:

: 140420-69-5
allyl α-D-xylopyranoside

: 334536-13-9
(2-hydroxy-ethyl) 2,3-di-O-benzyl-4-O-(tert-butoxycarbonylmethyl)-α-D-xylopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: NaH / dimethylformamide / 16 h / 20 °C

2: 97 percent / NaH / dimethylformamide / 16 h

3: 98 percent / O₃; NaBH₄ / methanol; tetrahydrofuran

With sodium tetrahydroborate; sodium hydride; ozone; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; 1: etherification / 2: etherification / 3: ozonolysis; reduction;
DOI:10.1016/S0968-0896(00)00256-X