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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173824Generated: November 2, 2026

Methanesulfonyl chloride → Methyl 6-(1-(methylsulfonyloxy)ethyl)nicotinate

https://huagongshe.com/reaction/2173824

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantMethyl 6-(1-hydroxyethyl)nicotinateHCID 66803327—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductMethyl 6-(1-(methylsulfonyloxy)ethyl)nicotinateHCID 8854163693.6%

Reaction Steps

To a 0° C. solution of methyl 6-(1-hydroxyethyl)nicotinate (0.100 g, 0.552 mmol) and 4-dimethylaminopyridine (152 mg, 1.32 mmol) in dichloromethane (10 mL) was added methanesulfonyl chloride (75.9 mg, 0.662 mmol) dropwise. The resulting mixture was stirred at room temperature for 1 hour. Additional methanesulfonyl chloride (75.9 mg, 0.662 mmol) was added and the mixture stirred at room temperature for an additional 2 hours. The mixture was quenched with water and extracted with dichloromethane. The organic layer was dried over sodium sulfate, filtered and concentrated to give crude methyl 6-(1-(methylsulfonyloxy)ethyl)nicotinate (134 mg) as an oil which was used in the next step directly.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056834B2
Source datasetuspto-grants-2015_06
ORD IDord-3d4ced23b9db49c7859c35c6cafc5848
Source noteuspto-grants-2015_06