(2R,4aR,6R,7S,8S,8aR)-8-Benzyloxy-2-phenyl-7-prop-2-ynyloxy-6-((2R,3R,4S,5R,6S)-3,4,5-tris-benzyloxy-6-methoxy-tetrahydro-pyran-2-ylmethoxy)-hexahydro-pyrano[3,2-d][1,3]dioxine

Base Information

Chemical Name:(2R,4aR,6R,7S,8S,8aR)-8-Benzyloxy-2-phenyl-7-prop-2-ynyloxy-6-((2R,3R,4S,5R,6S)-3,4,5-tris-benzyloxy-6-methoxy-tetrahydro-pyran-2-ylmethoxy)-hexahydro-pyrano[3,2-d][1,3]dioxine
CAS No.:887471-16-1
Molecular Formula:C₅₁H₅₄O₁₁
Molecular Weight:842.983
Hs Code.:

(2R,4aR,6R,7S,8S,8aR)-8-Benzyloxy-2-phenyl-7-prop-2-ynyloxy-6-((2R,3R,4S,5R,6S)-3,4,5-tris-benzyloxy-6-methoxy-tetrahydro-pyran-2-ylmethoxy)-hexahydro-pyrano[3,2-d][1,3]dioxine

Synonyms:(2R,4aR,6R,7S,8S,8aR)-8-Benzyloxy-2-phenyl-7-prop-2-ynyloxy-6-((2R,3R,4S,5R,6S)-3,4,5-tris-benzyloxy-6-methoxy-tetrahydro-pyran-2-ylmethoxy)-hexahydro-pyrano[3,2-d][1,3]dioxine

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Chemical Property of (2R,4aR,6R,7S,8S,8aR)-8-Benzyloxy-2-phenyl-7-prop-2-ynyloxy-6-((2R,3R,4S,5R,6S)-3,4,5-tris-benzyloxy-6-methoxy-tetrahydro-pyran-2-ylmethoxy)-hexahydro-pyrano[3,2-d][1,3]dioxine

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Technology Process of (2R,4aR,6R,7S,8S,8aR)-8-Benzyloxy-2-phenyl-7-prop-2-ynyloxy-6-((2R,3R,4S,5R,6S)-3,4,5-tris-benzyloxy-6-methoxy-tetrahydro-pyran-2-ylmethoxy)-hexahydro-pyrano[3,2-d][1,3]dioxine

There total 4 articles about (2R,4aR,6R,7S,8S,8aR)-8-Benzyloxy-2-phenyl-7-prop-2-ynyloxy-6-((2R,3R,4S,5R,6S)-3,4,5-tris-benzyloxy-6-methoxy-tetrahydro-pyran-2-ylmethoxy)-hexahydro-pyrano[3,2-d][1,3]dioxine 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:

: 887471-11-6
phenyl 4,6-O-benzylidene-3-O-benzyl-2-O-(prop-2-ynyl)-1-thio-α-D-mannopyranoside

: 53008-65-4,641635-63-4
methyl 2,3,4-tri-O-benzyl-D-glucopyranoside

: 887471-16-1
(2R,4aR,6R,7S,8S,8aR)-8-Benzyloxy-2-phenyl-7-prop-2-ynyloxy-6-((2R,3R,4S,5R,6S)-3,4,5-tris-benzyloxy-6-methoxy-tetrahydro-pyran-2-ylmethoxy)-hexahydro-pyrano[3,2-d][1,3]dioxine

: (2R,4aR,6S,7S,8S,8aR)-8-Benzyloxy-2-phenyl-7-prop-2-ynyloxy-6-((2R,3R,4S,5R,6S)-3,4,5-tris-benzyloxy-6-methoxy-tetrahydro-pyran-2-ylmethoxy)-hexahydro-pyrano[3,2-d][1,3]dioxine

Guidance literature:: phenyl 4,6-O-benzylidene-3-O-benzyl-2-O-(prop-2-ynyl)-1-thio-α-D-mannopyranoside; With 1-benzenesulfinyl piperidine; trifluoromethanesulfonic acid anhydride; 2,4,6-tri-tert-butylpyrimidine; In dichloromethane; at -60 ℃; for 0.5h;

methyl 2,3,4-tri-O-benzyl-D-glucopyranoside; In dichloromethane; at -60 ℃; for 2h;
DOI:10.1021/jo0526789

Reference yield:

: 100-39-0
benzyl bromide

: 887471-16-1
(2R,4aR,6R,7S,8S,8aR)-8-Benzyloxy-2-phenyl-7-prop-2-ynyloxy-6-((2R,3R,4S,5R,6S)-3,4,5-tris-benzyloxy-6-methoxy-tetrahydro-pyran-2-ylmethoxy)-hexahydro-pyrano[3,2-d][1,3]dioxine

Guidance literature:: Multi-step reaction with 3 steps

1.1: Bu₂SnO / toluene

1.2: 91 percent / CsF / toluene; dimethylformamide

2.1: 95 percent / NaH / dimethylformamide; various solvent(s); toluene / 3 h

3.1: 1-benzenesulfinyl piperidine; 2,4,6-tri-tert-butylpyrimidine; trifluoromethanesulfonic anhydride / CH₂Cl₂ / 0.5 h / -60 °C

3.2: CH₂Cl₂ / 2 h / -60 °C

With 1-benzenesulfinyl piperidine; sodium hydride; di(n-butyl)tin oxide; trifluoromethanesulfonic acid anhydride; 2,4,6-tri-tert-butylpyrimidine; In dichloromethane; N,N-dimethyl-formamide; toluene;
DOI:10.1021/jo0526789

Reference yield:

: 158716-07-5
phenyl 3-O-benzyl-4,6-O-benzylidene-1-thio-α-D-mannopyranoside

: 887471-16-1
(2R,4aR,6R,7S,8S,8aR)-8-Benzyloxy-2-phenyl-7-prop-2-ynyloxy-6-((2R,3R,4S,5R,6S)-3,4,5-tris-benzyloxy-6-methoxy-tetrahydro-pyran-2-ylmethoxy)-hexahydro-pyrano[3,2-d][1,3]dioxine

Guidance literature:: Multi-step reaction with 2 steps

1.1: 95 percent / NaH / dimethylformamide; various solvent(s); toluene / 3 h

2.1: 1-benzenesulfinyl piperidine; 2,4,6-tri-tert-butylpyrimidine; trifluoromethanesulfonic anhydride / CH₂Cl₂ / 0.5 h / -60 °C

2.2: CH₂Cl₂ / 2 h / -60 °C

With 1-benzenesulfinyl piperidine; sodium hydride; trifluoromethanesulfonic acid anhydride; 2,4,6-tri-tert-butylpyrimidine; In dichloromethane; N,N-dimethyl-formamide; toluene;
DOI:10.1021/jo0526789