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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 401801Generated: October 25, 2026

Water → Tert-butyl 3-((cyclopropylmethoxy)methyl)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/401801

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant(Chloromethyl)cyclopropaneHCID 80013—
Reactanttert-Butyl 3-(hydroxymethyl)pyrrolidine-1-carboxylateHCID 5237175—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 3-((cyclopropylmethoxy)methyl)pyrrolidine-1-carboxylateHCID 5773211384.1%

Reaction Steps

To a solution of tert-butyl 3-(hydroxymethyl)pyrrolidine-1-carboxylate (Preparation 65, 46.6 g, 0.232 mol, 1 eq) in anhydrous dimethylformamide (250 mL) was added in portions with stirring and under an atmosphere of argon a dispersion in oil of sodium hydride (11.2 g, 0.28 mol, 1.2 eq) in oil. The mixture was stirred for 45 min and then (chloromethyl)cyclopropane (26 mL, 0.28 mol, 1.2 eq) in anhydrous THF (30 mL) was added. The mixture was stirred for 12 h and then treated with water (100 mL) and extracted with ether (3×200 mL). Ether fractions were washed with water (2×100 mL), dried over sodium sulfate and evaporated. The residue was subjected to chromatography (chloroform/ethylacetate 10:1) on silica to afford title compound (50 g, 0.195 mol, 84%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741934B2
Source datasetuspto-grants-2014_06
ORD IDord-82323647352c41ca9b564354b465a54c
Source noteuspto-grants-2014_06