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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571312Generated: November 1, 2026

Methanesulfonyl chloride → HCID 86681720, compound

https://huagongshe.com/reaction/571312

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 86681719HCID 86681719—
SolventPyridineHCID 1049—
ProductHCID 86681720HCID 8668172088%

Reaction Steps

To a solution of benzyl 2-(5-amino-1,3-dioxoisoindolin-2-yl)acetate (1.0 g, 3.22 mmol) in pyridine (8 ml) cooled to 0° C., methanesulfonyl chloride (0.377 ml, 4.83 mmol) was added drop wise, and the resulting mixture was stirred at room temperature for 3 hours. The solvent was removed under vacuum and the residue was partitioned between 2N HCl and DCM; the aqueous phase was extracted with DCM and the combined organic layers were dried over Na2SO4 and evaporated to dryness. The crude was triturated with Et2O (15 ml) to give benzyl 2-(5-(methylsulfonamido)-1,3-dioxoisoindolin-2-yl)acetate (1.1 g, 2.83 mmol, 88% yield, MS/ESI+ 388.8 [MH]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09024027B2
Source datasetuspto-grants-2015_05
ORD IDord-8f7dbaba178641d790cda12a62d179fa
Source noteuspto-grants-2015_05