ethyl 3,4-di-O-benzyl-2,6-dideoxy-1-C-ethoxy-L-arabino-hexopyranoside

Base Information

Chemical Name:ethyl 3,4-di-O-benzyl-2,6-dideoxy-1-C-ethoxy-L-arabino-hexopyranoside
CAS No.:150367-56-9
Molecular Formula:C₂₄H₃₂O₅
Molecular Weight:400.515
Hs Code.:

Synonyms:ethyl 3,4-di-O-benzyl-2,6-dideoxy-1-C-ethoxy-L-arabino-hexopyranoside

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Chemical Property of ethyl 3,4-di-O-benzyl-2,6-dideoxy-1-C-ethoxy-L-arabino-hexopyranoside

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Technology Process of ethyl 3,4-di-O-benzyl-2,6-dideoxy-1-C-ethoxy-L-arabino-hexopyranoside

There total 4 articles about ethyl 3,4-di-O-benzyl-2,6-dideoxy-1-C-ethoxy-L-arabino-hexopyranoside 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:

: 117249-17-9
3,4-di-O-benzyl-L-rhamnal

: 150367-56-9
ethyl 3,4-di-O-benzyl-2,6-dideoxy-1-C-ethoxy-L-arabino-hexopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: pyrdinium chlorochromate / CH₂Cl₂ / ultrasound

2: 1) Et₃OBF₄, 2) Na / multistep reaction; other benzyl ether protected 2-deoxy-aldono-1,5-lactone; synthesis of carbohydrate ortholactones

With triethyloxonium fluoroborate; sodium; pyridinium chlorochromate; In dichloromethane;

Reference yield:

: 53657-42-4
L-rhamnal

: 150367-56-9
ethyl 3,4-di-O-benzyl-2,6-dideoxy-1-C-ethoxy-L-arabino-hexopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: 1) NaH, DMSO / 1) 1 h, 2) r. t., 3 h

2: pyrdinium chlorochromate / CH₂Cl₂ / ultrasound

3: 1) Et₃OBF₄, 2) Na / multistep reaction; other benzyl ether protected 2-deoxy-aldono-1,5-lactone; synthesis of carbohydrate ortholactones

With triethyloxonium fluoroborate; sodium; sodium hydride; dimethyl sulfoxide; pyridinium chlorochromate; In dichloromethane;

Reference yield:

: 34819-86-8
3,4-di-O-acetyl-6-deoxy-L-glucal

: 150367-56-9
ethyl 3,4-di-O-benzyl-2,6-dideoxy-1-C-ethoxy-L-arabino-hexopyranoside

Guidance literature:: Multi-step reaction with 4 steps

1: NaOMe, MeOH

2: 1) NaH, DMSO / 1) 1 h, 2) r. t., 3 h

3: pyrdinium chlorochromate / CH₂Cl₂ / ultrasound

4: 1) Et₃OBF₄, 2) Na / multistep reaction; other benzyl ether protected 2-deoxy-aldono-1,5-lactone; synthesis of carbohydrate ortholactones

With methanol; sodium methylate; triethyloxonium fluoroborate; sodium; sodium hydride; dimethyl sulfoxide; pyridinium chlorochromate; In dichloromethane;