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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 516139Generated: October 30, 2026

Triethylamine → Tert-butyl 3-(methanesulfonyloxy)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/516139

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant1-Boc-3-pyrrolidinolHCID 4416939—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
ProductTert-butyl 3-(methanesulfonyloxy)pyrrolidine-1-carboxylateHCID 4139999—

Reaction Steps

N-Boc-3-pyrrolidinol (1000 mg) was dissolved in chloroform (20 ml). Triethylamine (1.15 ml) and methanesulfonyl chloride (498 μl) were added thereto at 0° C. After stirring at room temperature for 1.0 hour, ethyl acetate and water were added thereto to separate the organic layer. After being washed with a saturated aqueous sodium bicarbonate solution, a saturated aqueous ammonium chloride solution and water, the organic layer was dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure to obtain the title compound as a colorless, oily compound (1.2 g). Physical properties: m/z [M+H]+ 266.1

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108973B2
Source datasetuspto-grants-2015_08
ORD IDord-705913ace0f9428e984fc2a96196d474
Source noteuspto-grants-2015_08