HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2231625Generated: November 2, 2026
Methanesulfonyl chloride → HCID 247764, compound
https://huagongshe.com/reaction/2231625
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (-)-2,3-O-Isopropylidene-D-threitol | HCID 785244 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 247764 | HCID 247764 | 66% |
Reaction Steps
The starting material (1) (3,4-O-isopropylidene-D-mannitol) was reacted with sodium periodate and potassium borohydride as described in J. Chem. Soc., Perkin Trans. I., 1972, 275 (the contents of which are herein incorporated by reference) to yield compound (2) in 92% yield. Compound (2) (5.1 g) was dissolved in pyridine (40 ml) and cooled in ice. To this solution was added methanesulphonyl chloride (18 ml), dropwise with stirring. The mixture was allowed to stand at room temperature for 3 hours, after which time it was added to a solution of sodium bicarbonate. This solution was then extracted with dichloromethane (5×50 ml) and the combined extracts were dried (MgSO4) and concentrated in vacuo. The residue obtained was recrystallised from ethanol to give 2,3-O-isopropylidene-1,4-di-O-methanesulphonyl-D-threitol (3), (6.6 g, 66%), m.p. 83°-85° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04783452 |
|---|
| Source dataset | uspto-grants-1988_11 |
|---|
| ORD ID | ord-00b19121bf104c5b9bddcf2665e67340 |
|---|
| Source note | uspto-grants-1988_11 |
|---|