HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707949Generated: November 1, 2026
4-O-benzoyl-3,5-di-O-benzyl-2-deoxy-L-threo-pentose dibenzyl dithioacetal → 3,5-di-O-benzyl-2-deoxy-L-threo-pentose dibenzyl dithioacetal
https://huagongshe.com/reaction/1707949
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-O-benzoyl-3,5-di-O-benzyl-2-deoxy-L-threo-pentose dibenzyl dithioacetal | HCID 10886810 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3,5-di-O-benzyl-2-deoxy-L-threo-pentose dibenzyl dithioacetal | HCID 15059957 | — |
Reaction Steps
To a solution of 4-O-benzoyl-3,5-di-O-benzyl-2-deoxy-L-threo-pentose dibenzyl dithioacetal (88.8 g, 137 mmol) in dichloromethane (500 ml) was added a solution of sodium methoxide (11.1 g, 206 mmol) in methanol (205 ml) dropwise, with stirring, at 0° C. The reaction mixture was then allowed to warm to room temperature over a period of 3 hours. At the end of this time TLC (hexane-ethyl acetate [4:1]) revealed complete conversion to a slower moving component (Rf 0.31). The mixture was then poured into a 5% solution of NaH2PO4 and extracted with dichloromethane. The dichloromethane extracts were then washed with a 5% solution of sodium hydrogen carbonate and water, dried (magnesium sulphate) and evaporated. The crude title product was applied to a silica gel column eluted with hexane-ethyl acetate (4:1). Combination of the appropriate fractions gave the title product as a clear colourless syrup.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05356882 |
|---|
| Source dataset | uspto-grants-1994_10 |
|---|
| ORD ID | ord-59f9c9fc71294a27828e4a3a45e757a1 |
|---|
| Source note | uspto-grants-1994_10 |
|---|