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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 714225Generated: October 25, 2026

Nitrogen → 4-(Benzyloxy)-1-(pyrrolidin-1-yl)butan-1-one

https://huagongshe.com/reaction/714225

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantPyrrolidineHCID 31268—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-(Benzyloxy)butanoic acidHCID 562201—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product4-(Benzyloxy)-1-(pyrrolidin-1-yl)butan-1-oneHCID 49371180—

Reaction Steps

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of 4-benzyloxybutyric acid (246 mg, 1.27 mmol), pyrrolidine (0.13 mL, 1.52 mmol), EDC.HCl (493 mg, 2.53 mmol), HOBt (262 mg, 1.90 mL) and DIPEA (0.65 mL, 3.80 mmol) in CH2Cl2 (10 mL) was heated at rt until completion of the reaction. Water was added, the layers separated and the aq. layer extracted with CH2Cl2 (2×). The combined org. extracts were washed with brine, dried (MgSO4), filtered and concentrated under reduced pressure. The crude residue was purified by FC (hept-EA, 1:0→0:1) to give 4-(benzyloxy)-1-(pyrrolidin-1-yl)butan-1-one as a colorless oil. LC-MS-conditions 08: tR=0.77 min; [M+H]+=247.95.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187435B2
Source datasetuspto-grants-2015_11
ORD IDord-e41d7a5469574e83ac8fe401c5c1d186
Source noteuspto-grants-2015_11