methyl 5-O-(tert-butyldiphenylsilyl)-2-deoxy-α,β-D-threo-pentofuranoside

Base Information

Chemical Name:methyl 5-O-(tert-butyldiphenylsilyl)-2-deoxy-α,β-D-threo-pentofuranoside
CAS No.:791084-51-0
Molecular Formula:C₂₂H₃₀O₄Si
Molecular Weight:386.563
Hs Code.:

Synonyms:methyl 5-O-(tert-butyldiphenylsilyl)-2-deoxy-α,β-D-threo-pentofuranoside

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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 methyl 5-O-(tert-butyldiphenylsilyl)-2-deoxy-α,β-D-threo-pentofuranoside

Chemical Property:

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Technology Process of methyl 5-O-(tert-butyldiphenylsilyl)-2-deoxy-α,β-D-threo-pentofuranoside

There total 9 articles about methyl 5-O-(tert-butyldiphenylsilyl)-2-deoxy-α,β-D-threo-pentofuranoside 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:

: 40156-61-4
5,5-dimethoxy-pent-2t-en-1-ol

: 791084-51-0
methyl 5-O-(tert-butyldiphenylsilyl)-2-deoxy-α,β-D-threo-pentofuranoside

Guidance literature:: Multi-step reaction with 3 steps

1: 87 percent / DMAP, Et₃N

2: 81 percent / K₂OsO₂(OH)2, K₂CO₃, MeSONH₂ / (DHQD)2PHAL / H₂O; 2-methyl-propan-2-ol

3: dild. HCl / CH₂Cl₂

With hydrogenchloride; dmap; methanesulfinamide; K₂OsO₂(OH)2; potassium carbonate; triethylamine; 1,4-bis(9-O-dihydroquinidine)phthalazine; In dichloromethane; water; tert-butyl alcohol;
DOI:10.1016/S0040-4039(00)73487-3

Reference yield:

: 79576-62-8
5-hydroxy-pent-3-ynal-dimethylacetal

: 791084-51-0
methyl 5-O-(tert-butyldiphenylsilyl)-2-deoxy-α,β-D-threo-pentofuranoside

Guidance literature:: Multi-step reaction with 4 steps

1: 80 percent / LiAlH₄ / tetrahydrofuran / Heating

2: 87 percent / DMAP, Et₃N

3: 81 percent / K₂OsO₂(OH)2, K₂CO₃, MeSONH₂ / (DHQD)2PHAL / H₂O; 2-methyl-propan-2-ol

4: dild. HCl / CH₂Cl₂

With hydrogenchloride; dmap; lithium aluminium tetrahydride; methanesulfinamide; K₂OsO₂(OH)2; potassium carbonate; triethylamine; 1,4-bis(9-O-dihydroquinidine)phthalazine; In tetrahydrofuran; dichloromethane; water; tert-butyl alcohol;
DOI:10.1016/S0040-4039(00)73487-3

Reference yield:

: 33639-45-1
3-butynal dimethyl acetal

: 791084-51-0
methyl 5-O-(tert-butyldiphenylsilyl)-2-deoxy-α,β-D-threo-pentofuranoside

Guidance literature:: Multi-step reaction with 5 steps

1: n-BuLi

2: 80 percent / LiAlH₄ / tetrahydrofuran / Heating

3: 87 percent / DMAP, Et₃N

4: 81 percent / K₂OsO₂(OH)2, K₂CO₃, MeSONH₂ / (DHQD)2PHAL / H₂O; 2-methyl-propan-2-ol

5: dild. HCl / CH₂Cl₂

With hydrogenchloride; dmap; lithium aluminium tetrahydride; n-butyllithium; methanesulfinamide; K₂OsO₂(OH)2; potassium carbonate; triethylamine; 1,4-bis(9-O-dihydroquinidine)phthalazine; In tetrahydrofuran; dichloromethane; water; tert-butyl alcohol;
DOI:10.1016/S0040-4039(00)73487-3