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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1723696Generated: November 2, 2026

Methanesulfonyl chloride → HCID 24728873, compound

https://huagongshe.com/reaction/1723696

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant(3R,4R)-1-Benzylpyrrolidine-3,4-diolHCID 7021491—
SolventDichloromethaneHCID 6344—
ProductHCID 24728873HCID 2472887367.6%

Reaction Steps

To an ice-cold (0-5° C.) solution of the product from Step 2 (5.27 g, 27.3 mmol) and TEA (8.27 g, 81.9 mmol) in dichloromethane (50 mL), was added methanesulfonyl chloride (6.87 g, 60.0 mmol) over a period of 30 minutes. After stirring at RT overnight, the reaction mixture was washed with water. The organic layer was dried (sodium sulfate), filtered, and concentrated to give the crude product which was purified over a silica column (5:95 EtOAc/hexane) to obtain pure product (6.44 g, 67.6%). 1H NMR (400 MHz, CDCl3) δ 7.32-7.26 (5H, m), 5.14 (2H, m), 3.65 (2H, s), 3.15-3.08 (2H, m), 3.08 (6H, s), 2.76 (2H, dd). MS m/z 350 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07485641B2
Source datasetuspto-grants-2009_02
ORD IDord-329f4c7d8f664b418841d0481141ec67
Source noteuspto-grants-2009_02