HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 440712Generated: October 26, 2026
Methanesulfonyl chloride → 3,5-di-O-benzyl-2-deoxy-4-O-methane-sulphonyl-L-threo-pentose dibenzyl dithioacetal
https://huagongshe.com/reaction/440712
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 3,5-di-O-benzyl-2-deoxy-L-threo-pentose dibenzyl dithioacetal | HCID 15059957 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 3,5-di-O-benzyl-2-deoxy-4-O-methane-sulphonyl-L-threo-pentose dibenzyl dithioacetal | HCID 15059960 | — |
Reaction Steps
To a solution of 3,5-di-O-benzyl-2-deoxy-L-threo-pentose dibenzyl dithioacetal (61.4 g, 113 mmol) in dry pyridine (700 ml) was added methanesulphonyl chloride (19.4 g, 169 mmol) in dry pyridine (200 ml) dropwise, with stirring, at 0° C. The temperature of the mixture was raised to room temperature and stirring continued for 18 hours. The pyridine was then removed in vacuo and the residue dissolved in dichloromethane. The dichloromethane extracts were then successively washed with 2M hydrochloric acid, 1M sodium carbonate and water, dried (magnesium sulphate) and evaporated to give the title product as a thick viscous syrup. A sample of this was crystallised from hexane-ethyl acetate to give the title product as white crystals, m.p 82°-83° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05521163 |
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| Source dataset | uspto-grants-1996_05 |
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| ORD ID | ord-c9b256705bed443288b6f29296ee4bdd |
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| Source note | uspto-grants-1996_05 |
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