3-O-benzyl-1,2-O-isopropylidene-5-S-phenyl-5-thio-α-D-xylofuranose

Base Information

• Chemical Name: 3-O-benzyl-1,2-O-isopropylidene-5-S-phenyl-5-thio-α-D-xylofuranose
• CAS No.: 157555-89-0
• Molecular Formula: C₂₁H₂₄O₄S
• Molecular Weight: 372.485
• Mol file: 157555-89-0.mol

Synonyms:3-O-benzyl-1,2-O-isopropylidene-5-S-phenyl-5-thio-α-D-xylofuranose

Chemical Property of 3-O-benzyl-1,2-O-isopropylidene-5-S-phenyl-5-thio-α-D-xylofuranose

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 3-O-benzyl-1,2-O-isopropylidene-5-S-phenyl-5-thio-α-D-xylofuranose

There total 1 articles about 3-O-benzyl-1,2-O-isopropylidene-5-S-phenyl-5-thio-α-D-xylofuranose 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: 86.0%

thiophenol (108-98-5) + 3-O-benzoyl-1,2-O-isopropylidene-5-O-p-toluenesulfonyl-α-D-xylofuranose (69434-49-7) → 3-O-benzyl-1,2-O-isopropylidene-5-S-phenyl-5-thio-α-D-xylofuranose (157555-89-0)

Guidance literature:

With 1,8-diazabicyclo[5.4.0]undec-7-ene; In benzene; for 12h; Ambient temperature;

Reference yield: 99.0%

3-O-benzyl-1,2-O-isopropylidene-5-S-phenyl-5-thio-α-D-xylofuranose (157555-89-0) → 3-O-benzyl-5-chloro-1,2-O-isopropylidene-5-S-phenyl-5-thio-α-D-xylofuranose

Guidance literature:

With tetrachloromethane; N-chloro-succinimide; for 4h; Ambient temperature;

Reference yield:

3-O-benzyl-1,2-O-isopropylidene-5-S-phenyl-5-thio-α-D-xylofuranose (157555-89-0) → (3aR,5S,6R,6aR)-2,2-dimethyl-5-(phenylthiomethyl)-tetrahydrofuro[2,3-d][1,3]dioxol-6-ol (157555-88-9)

Guidance literature:

Multi-step reaction with 2 steps

1: 99 percent / CCl₄, NCS / 4 h / Ambient temperature

2: 65 percent / TiCl₄ / CH₂Cl₂ / 0.25 h / -23 °C

With tetrachloromethane; N-chloro-succinimide; titanium tetrachloride; In dichloromethane;

upstream raw materials:

thiophenol

3-O-benzoyl-1,2-O-isopropylidene-5-O-p-toluenesulfonyl-α-D-xylofuranose

Downstream raw materials:

(3aR,5S,6R,6aR)-2,2-dimethyl-5-(phenylthiomethyl)-tetrahydrofuro[2,3-d][1,3]dioxol-6-ol