Methyl 5-O-(tert-butyldiphenylsilyl)-2,6-dideoxy-α-L-lyxo-hexafuranoside

Base Information

Chemical Name:Methyl 5-O-(tert-butyldiphenylsilyl)-2,6-dideoxy-α-L-lyxo-hexafuranoside
CAS No.:161606-75-3
Molecular Formula:C₂₃H₃₂O₄Si
Molecular Weight:400.59
Hs Code.:

Synonyms:Methyl 5-O-(tert-butyldiphenylsilyl)-2,6-dideoxy-α-L-lyxo-hexafuranoside

Suppliers and Price of Methyl 5-O-(tert-butyldiphenylsilyl)-2,6-dideoxy-α-L-lyxo-hexafuranoside

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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)-2,6-dideoxy-α-L-lyxo-hexafuranoside

Chemical Property:

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Technology Process of Methyl 5-O-(tert-butyldiphenylsilyl)-2,6-dideoxy-α-L-lyxo-hexafuranoside

There total 9 articles about Methyl 5-O-(tert-butyldiphenylsilyl)-2,6-dideoxy-α-L-lyxo-hexafuranoside 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:

: 113666-60-7
methyl 2-deoxy-3-O-benzyl-β-D-erythro-pentofuranoside

: 161606-75-3
Methyl 5-O-(tert-butyldiphenylsilyl)-2,6-dideoxy-α-L-lyxo-hexafuranoside

Guidance literature:: Multi-step reaction with 5 steps

1: 1.) (COCl)2, DMSO, 2.) NEt₃ / 1.) CH₂Cl₂, ca. -50 deg C, 15 min, 2.) ca. -50 deg C to 20 deg C

2: diethyl ether / -70 °C

3: 100 percent / pyridine, imidazole / 17 h / 20 °C

4: NBS, aq. CaCO₃ / CCl₄ / 0.5 h / 20 - 25 °C / Irradiation

5: KOH / methanol / 18 h / Ambient temperature

With pyridine; 1H-imidazole; potassium hydroxide; N-Bromosuccinimide; oxalyl dichloride; dimethyl sulfoxide; triethylamine; calcium carbonate; In methanol; tetrachloromethane; diethyl ether;
DOI:10.1021/jo00106a035

Reference yield:

: 105454-48-6
3-O-Benzyl-2-deoxy-5-(triphenylmethyl)-D-erythro-pentofuranoside

: 161606-75-3
Methyl 5-O-(tert-butyldiphenylsilyl)-2,6-dideoxy-α-L-lyxo-hexafuranoside

Guidance literature:: Multi-step reaction with 6 steps

1: methanolic HCl / 3.5 h / 20 °C

2: 1.) (COCl)2, DMSO, 2.) NEt₃ / 1.) CH₂Cl₂, ca. -50 deg C, 15 min, 2.) ca. -50 deg C to 20 deg C

3: diethyl ether / -70 °C

4: 100 percent / pyridine, imidazole / 17 h / 20 °C

5: NBS, aq. CaCO₃ / CCl₄ / 0.5 h / 20 - 25 °C / Irradiation

6: KOH / methanol / 18 h / Ambient temperature

With pyridine; 1H-imidazole; hydrogenchloride; potassium hydroxide; N-Bromosuccinimide; oxalyl dichloride; dimethyl sulfoxide; triethylamine; calcium carbonate; In methanol; tetrachloromethane; diethyl ether;
DOI:10.1021/jo00106a035

Reference yield:

: 161661-39-8
Methyl 3-O-benzyl-2-deoxy-5-β-D-erythro-pentodialdo-1,4-furanoside

: 161606-75-3
Methyl 5-O-(tert-butyldiphenylsilyl)-2,6-dideoxy-α-L-lyxo-hexafuranoside

Guidance literature:: Multi-step reaction with 4 steps

1: diethyl ether / -70 °C

2: 100 percent / pyridine, imidazole / 17 h / 20 °C

3: NBS, aq. CaCO₃ / CCl₄ / 0.5 h / 20 - 25 °C / Irradiation

4: KOH / methanol / 18 h / Ambient temperature

With pyridine; 1H-imidazole; potassium hydroxide; N-Bromosuccinimide; calcium carbonate; In methanol; tetrachloromethane; diethyl ether;
DOI:10.1021/jo00106a035