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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2275704Generated: October 31, 2026

Water → Tert-butyl 2-[(methanesulfonyloxy)methyl]pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/2275704

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactanttert-Butyl 2-(hydroxymethyl)pyrrolidine-1-carboxylateHCID 550865—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 2-[(methanesulfonyloxy)methyl]pyrrolidine-1-carboxylateHCID 18007568—

Reaction Conditions

Temperature-20 °C

Reaction Steps

To a solution of tert-butyl 2-(hydroxymethyl)pyrrolidine-1-carboxylate (1.0 g, 5.0 mmol) and TEA (1.0 g, 9.9 mmol) in CH2Cl2 (40 mL) was slowly added MsCl (0.63 g, 5.5 mmol). The reaction mixture was stirred for 30 min at −20° C. and then water (60 mL) was added. The aqueous phase was separated and extracted with CH2Cl2. The combined organic layers were washed with brine, dried over Na2SO4, filtered, and concentrated under reduced pressure to afford the crude tert-butyl 2-((methylsulfonyloxy)methyl)pyrrolidine-1-carboxylate that was used directly without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126940B2
Source datasetuspto-grants-2015_09
ORD IDord-e99034a380a54f8c9f06edbf84196867
Source noteuspto-grants-2015_09